Prices from
£490
Our Expert Scan & NIPT tests are competitively priced.
Panorama NIPT
Non-invasive prenatal test
We combine advanced Panorama NIPT for Down’s syndrome and chromosomal anomalies with our expert ultrasound scans to check your baby’s health as early as possible.
Prices from
£490
Our Expert Scan & NIPT tests are competitively priced.
Best from
10 weeks
NIPT with early structural assessment.
5★ rated
service
Google, Trustpilot & Doctify.
Timing
At London Pregnancy Clinic, we offer the most advanced Panorama AI NIPT packages offering not only panorama screening test for Down’s, Edward’s and Patau’s Syndromes, but also a comprehensive structural screening of your baby from 9 weeks.
We recommend booking your NIPT along with our revolutionary 10 Week scan (10-11 week scan).
It is possible to perform a Panorama Test during pregnancy from 9 weeks, however, structural assessment of your baby by ultrasound at this embryonic stage can be limited.
If you are past the 9-11 week mark, visit our Scans Page to find out which fetal scan you will be having along with NIPT, as the test is available from 10-24 weeks.

Summary
NIPT explained
Non-Invasive Prenatal Screening is a blood test for advanced screening test predominantly for three chromosomal anomalies:
Natera reports over 99% combined sensitivity for these three trisomies in the SMART study.
The figures above are the published detection rates for the Panorama NIPT.
The test is highly accurate with false positive rates <0.1% for all 3 trisomies. The test can also detect the Fetal Sex with >99% accuracy.
Why 10 weeks?
Providers
‘Harmony Test‘ is a brand name for Roche’s NIPT. The test was developed by startup Ariosa (US) more than 10 years ago. Currently the analysis performed in London by TDL Genetics.
‘Panorama AI’ is a test developed by Natera (US), a pioneer in the field. New upgraded Panorama AI algorithm uses combination of artificial intelligence (AI) with Natera’s proprietary genetic methodology to improve both accuracy and the positive predictive value for extended range of genetic conditions.
The Harmony test was discontinued in the UK in 2023. Its laboratory, The Doctors Laboratory (TDL) in London, now runs TDL VeriSeq V2 in its place — a modern Illumina assay screening for Down’s (T21), Edwards’ (T18) and Patau’s (T13) syndromes with optional fetal sex, reporting in 2–4 working days at £540 with your scan.
Please find a comparison table between the tests below.
Appointment flow
Our specialists will initially conduct an anatomical examination of the baby to check for structural anomalies and take some measurements for the NIPT test.
Once the clinician is satisfied with the baby’s normal structural examination, they will proceed with a consultation about NIPT to answer your questions about every aspect of the test.
Finally, our friendly phlebotomist will take a blood sample from the mother’s arm – just like any routine blood test you may have done elsewhere.
Our staff then process the blood samples and will send them to the lab soon after your appointment. Now all there’s left to do is to wait for a call from us!
Scan + NIPT

Ultrasound is a vital part of fetal screening. The laboratory requires a confirmation of viability and gestational age by the clinic submitting each NIPT
NIPT is a highly effective screening test for 3 chromosomal anomalies plus some other conditions (Panorama only), however it is unable to screen for structural anomalies such as heart or brain defects which are more common and often more serious than Down’s Syndrome.
Here at London Pregnancy Clinic we specialise in early detection of fetal anomalies, the fetal heart and brain. We can detect some of the most severe fetal anomalies as early as 10 weeks. Visit our Scans Page to find out which scan you will be having along with NIPT. Generally, we believe that our 10 Weeks Scan is the best option.
If you choose to have the Panorama Test at 9 weeks, we will also perform an expert structural scan for your baby (embryo), however, this scan will be understandably limited due to the small size and developmental immaturity of the baby.
Structural screening
With our expertise and technology we are able to screen for structural anomalies from 10 weeks (approximate prevalence in the first trimester):
In comparison, the prevalence of the chromosomal conditions screened for by NIPT:
Down’s Syndrome (1:700) · Edward’s Syndrome (1:1,400) · Patau’s Syndrome (1:5,000)
If you take the test at 12+ weeks we are able to screen by ultrasound for >100 structural fetal anomalies, however we may lose few advantages of early NIPT.
Counselling
We offer free pre-NIPT counselling with our viability scans. There are different NIPT options and making right choice can be very confusing. You also probably will need some time to consider your options. At our viability scan, after confirmation of normal development of your pregnancy , we will explain you how different non-invasive prenatal tests work, and you can choose which test is right for you.
Learn moreComparison
| Feature | PrenatalSafeEuroFins | Panorama AINatera | Smart Test — Knova®Fulgent |
|---|---|---|---|
| Package | Basic | Basic Extended | Most Advanced |
| As early as… | 10 weeks | 9 weeks | 10 weeks |
| Turnaround (working days) | 2–5 | 7–10 | 7–10 |
| Lab Location | UK | US | US |
| No-Call / Redraw rates | 0.5–2% | 1–3% | 0–1.5% |
| Down, Edwards & Patau Syndrome | |||
| Di George Syndrome (22q Del) | |||
| Triploidy | |||
| Turner Syndrome (45x) | |||
| Sex Chromosomes Aneuploidies | |||
| Additional Chromosomes | |||
| Microdeletions | 1 | 12 | |
| De Novo Genetic Syndromes | 56 genes | ||
| Twin Pregnancies | Without 22q del | ||
| Vanishing twin syndrome | |||
| Donor Eggs / Surrogacy | Without 22q del | ||
| Early Anomaly Ultrasound Screening | Basic | Basic | Comprehensive |
| Fetal Sex Reveal (Optional) | |||
| Scan & NIPT Price | £540 | £590 / £790 microdeletions | from £990** |
General Notes: The data taken from the clinical data published by EuroFins, Fulgent and Natera.
* Panorama AI for Di George Syndrome was validated in the largest prospective NIPT study (SMART; Dar et al., American Journal of Obstetrics and Gynecology, 2022). It combines artificial intelligence (AI) with Natera’s proprietary SNP-based methodology to improve both accuracy and the positive predictive value (PPV) for 22q deletions. The data from this study showed detection of all cases of the most common 2.5–3 Mb 22q11.2 deletion and 83% of all 22q11.2 deletions, with a 53% positive predictive value (PPV) and just a 0.05% false positive rate.
** Triploidy, Turner Syndrome (45X) and sex chromosome aneuploidy NIPT screening has limited clinical validation data. It can have higher false positive rate and also inconclusive results.
*** For twin pregnancies and egg donation, Panorama with DiGeorge screening is NOT an option. Please get in touch to enquire.
Frequently Asked Questions
It’s important for us that you understand the terminology we use for screening tests:
Detection rate is defined as the fraction of all patients who have the disease and are called positive by the screening test.
Positive Predictive Value or PPV is the proportion of the ‘true positives’ as proportion of all positive results. As a practical example, the Panorama AI test has a 95% PPV for Down’s Syndrome, meaning that 95% of the fetuses identified as ‘High Probability’ will statistically have the condition. However, this means that around 1 in 20 ‘High Probability’ results is a ‘false positive’, where the test returns a ‘High Probability’ result for a fetus that doesn’t have Down’s Syndrome. This is not the same as the overall false-positive rate, which is below 0.1% of all women tested (Gil et al., 2017), and the PPV for you depends on your age and background chance — you can model your own numbers with our NIPT PPV calculator.
That’s why, for every High Probability result we would refer the patient for a diagnostic test such as CVS or Amniocentesis to verify the results.
In the past there has been confusion about certain aspects of NIPT – please see this notice. If any of the above still unclear to you, please get in touch with us via email or phone and our friendly stuff will be happy to run you through the characteristics of the test.
We wrote a special blog post about understanding the statistics of the NIPT test, if you would like to find out more, click here.
Read more in our Blog
Non-Invasive Prenatal Testing (NIPT) or alternatively Non-Invasive Prenatal Screening (NIPS) is a screening method for determining the chance that a baby will be born with Down’s syndrome or other chromosomal anomalies. NIPT is based on the assessment of small DNA fragments from a baby’s placenta (named ‘cell-free DNA’ or ‘cfDNA’) that are disseminated in the blood of every pregnant mother. Placental cfDNA is usually identical to the DNA of the baby and testing it provides an opportunity for early detection of particular chromosomal anomalies without harming the baby.
Harmony Test is a well known NIPT brand by Ariosa/Roche. Harmony Prenatal Test is a trade name of the cfDNA test. We have experience of using Harmony for many years. Currently there are many other brands of NIPT, which provide similar or better performance. After careful consideration we have chosen our second NIPT provider which is Panorama AI.
Panorama AI NIPT (non invasive prenatal screening) is an advanced NIPT, based on state-of-the-art algorithms, it has lower sample failure rate comparing with Harmony Test and its price is more affordable for the future parents. The limitation of Panorama NIPT is its long results reporting time (up to 10 working days) which is a result of sample shipping to US based Lab.
Although cfDNA is a relatively new genetic test, it has been proven to be superior to any other screening tests for Down’s Syndrome, including the Combined Screening Test (CST) used by the NHS. However, NIPT can detect a relatively small proportion (about 15%) of all fetal anomalies, because the vast majority of fetal anomalies are physical (structural) and not chromosomal.
NIPT is a screening test, meaning that NIPT cannot give a definitive answer about whether a baby has Down’s syndrome or other tested chromosomal conditions. If the results are positive (high chance) follow-up invasive testing is needed to get a definite diagnosis. Any invasive testing carries a small risk of miscarriage.
22q deletion (del) syndrome or Di George syndrome is genetic condition which is caused by a small, missing or “deleted” piece of the 22nd chromosome. Unfortunately that missing piece can affect every system in the human body including heart (heart defects in 75% babies), palate, immune system, hormones, kidneys and others. It also can affect mental health and is associated with learning and behavioral differences, anxiety, and other mental health issues like schizophrenia (in 25% of adults).
Panorama AI can detect >80% of the fetuses with 22q del with positive predictive value of 53%. Early detection of 22q del can lead to earlier interventions and better outcomes for affected individuals. For instance in our clinic we can perform early fetal echocardiography from 12 weeks to exclude severe heart anomaly associated with 22q del.
For more information please visit www.22q.org
Read Our Blog
Currently NIPT is not routinely offered by the NHS.
The Nuchal Translucency (NT) thickness measurements scan was developed in the 1990s, and at the time was the best screening option for Down’s Syndrome offering about 62% accuracy and 5% false positive rate. The NHS now offers the ‘Combined Test’ at 11-14 weeks which includes a Nuchal Translucency scan along with a blood test (for PAPP-A and HCG proteins) with improved the accuracy of 81% and false positive rate of 4.5%.
NIPT was first introduced in 2011 and was shown to have superior accuracy to the Combined Test with an over 99% detection rate for Down’s syndrome and a false-positive rate below 0.1% (Gil et al., 2017). Please note, we still recommend following through with your NHS antenatal appointments, they are important for the continuity of your pregnancy care.
The Harmony test at London Pregnancy Clinic screens for the three most common chromosomal conditions in pregnancy: Down’s syndrome (trisomy 21), Edwards’ syndrome (trisomy 18) and Patau’s syndrome (trisomy 13). You can also choose to include fetal sex determination. These are the same three conditions covered by NHS screening, and Harmony reports each as a low-chance or high-chance result.
If you would like a wider panel, such as DiGeorge syndrome (22q deletion), sex chromosome differences or microdeletions, our Panorama AI test screens for more conditions. Every Harmony test is paired with an expert ultrasound scan, because NIPT cannot detect structural anomalies. Our specialists will help you choose the right test at your appointment; see our Harmony test page or read more about NIPT at London Pregnancy Clinic.
Some biotechnological companies/manufacturers of NIPT including Panorama AI, which London Pregnancy Clinic offers, have launched commercially available products aiming to screen for sex chromosome abnormalities and microdeletions (including 22q del).
Although the tests are technologically advanced, the peer-reviewed validation data for those tests is patchy and the accuracy is inferior to the tests for T21, T18 and T13.
In the UK, the NHS considers the use of those tests controversial and as such unlikely to accept a ‘high probability’ or ‘inconclusive’ test results as a referral for further invasive testing or genetic counselling.
We recommend to take the NIPT along with our comprehensive early anomaly scan (10 Weeks Scan) as soon as possible – 10 weeks. Early detection of either chromosomal or structural anomalies allows more time in terms of pregnancy management for those conditions. If your sample fails you have plenty time for redraw.
If you’re unsure about the age of your pregnancy, we strongly recommend to perform Viability Scan with us at around 7-8 weeks of your gestation. Viability scan will date your pregnancy and we can arrange earliest possible appointment for your NIPT.
If you prefer not to have Viability Scan please allow a couple of days after the 10 weeks mark to avoid repeat appointments for drawing the bloods. You can also miss all the advantages of 10 Weeks Scan, because your baby will be too young to have proper early anomaly scan.
In theory, NIPT is available from 9-40 weeks, but it is strongly recommended to take the test in the first trimester, as the pregnancy management options in the second trimester can be very limited.
Yes, you can. Panorama AI works from 9 weeks. Please note that in this case structural assessment of the baby by ultrasound can be limited and we will be unable to screen for some very serious conditions like holoprosencephaly or spina bifida. If you wish to have NIPT before 10 weeks, please consider scan from 9 weeks 4 days.
Following your scan appointment, you will receive a detail scan report from our doctors, as a hard copy and a PDF version sent to you via our secure cloud system Tricefy.
As soon as we receive your NIPT test results from the laboratory, our clinician reviews the test results and signs them off. One of our friendly clinical staff will then contact you via a phone call to interpret the test results. We will then send you a soft copy of the test results via Tricefy.
The Harmony Prenatal Test is not validated and can not be use for use in pregnancies with:
Please note that IVF pregnancies are eligible for Harmony Test
Turnaround time of Harmony Test in London is about 3-5 working days in 95% of the cases. For Panorama, the tests are sent over to the US and can take up to 5-9 working days.
From our clinic the sample is securely collected by a specialist medical courier service.
See below information about Harmony test no-call results and need to redraw the blood sample (no additional cost.)
The main advantages of NIPT are related to Down’s syndrome (T21) screening.
They are:
As any screening test NIPT has some disadvantages.
Here there are the most significant NIPT limitations:
The main advantages of the brand new Panorama Test AI algorithm compared with other NIPT providers are:
The main disadvantages of Panorama Test are:
In case the NIPT result is high chance for Down syndrome or other conditions our doctor will contact you and explain the further steps we advise to take. We will most likely arrange a referral to your NHS Fetal Medicine Unit for further counselling and possible diagnostic test such as CVS or amniocentesis.
Alternatively we can refer you to private Fetal Medicine Consultant (consultation cost is not included in our service).
We will also offer Early Fetal Echocardiography for free (regular cost of the examination £360) for all our patients with high chance NIPT for trisomy 21, Di George syndrome, trisomy 18, trisomy 13 and Turner syndrome.
Although the Harmony Test is very accurate, no screening test is diagnostic: a proportion of high-chance results for Down’s syndrome are false positives, where the baby does not in fact have Down’s syndrome. The exact chance depends on your age and background risk.
Biological factors with the potential to cause discordance between cfDNA results and baby’s genetic status include uncommon conditions like confined placental mosaicism, fetal mosaicism, maternal chromosome changes, and the presence of an unrecognised, nonviable (or viable) twin.
Most pregnant women receive complete results from cfDNA testing, indicating either a high or low probability for aneuploidy.
In about 3% of cases (much more common with Harmony test) we will need to contact you without giving you a test result and ask to come for additional sample of blood or to give us more information about your pregnancy or medical history. There will be no extra cost for additional blood test.
It is because in small proportion of blood specimens submitted after 10 weeks gestation there is insufficient amount of baby’s cfDNA. This situation called low fetal fraction. The chance to have low fetal fraction is getting higher with increased maternal body weight. There are other rare factors making NITP results inconclusive. Our guide to low fetal fraction and NIPT no-call results explains the causes and your options in more detail.
In the case of Harmony Test no-call results we will discuss with you options of alternative screening and/or referral for diagnostic testing if you either decline a second attempt at NIPT or do not receive a result after two attempts.
The Harmony scan can only be done from a gestational age of 10 weeks, while Panorama NIPT can be done from 9 weeks. TDL/Natera do not accept any blood samples for patients below that Gestational Age. We recommend waiting until a gestational age of 10 weeks + 2 days (9+4 for Panorama Test) to perform the Harmony/Panorama Scan to avoid having to come in more than once.
In case you booked for Panorama / Harmony Scan, but the ultrasound scan indicated a GA below 9/10 weeks (respectively), we will have to rearrange for you to come in at a later date for an additional cost of £50 to cover for our staffing cost.
In case of No-Call results from the test (about 3% of the cases), we will be happy to schedule in another time to draw another blood sample free of charge. In case of a second No-Call result, we will refund the Harmony Test portion of the appointment charge as per below. If, upon discussion with our clinician, you decide that the Harmony Test is not the right decision for you, we will refund the Harmony Test proportion of the appointment and will only charge for the scan.
In the case of inconclusive results for Downs syndrome or trisomies 18 or 13 we are committed to refund your for the Harmony Test cost.
Because the Harmony Test is being undertaken by third party – TDL (The Doctors Laboratory) we will contact them to arrange the refund. The refund will be for Harmony Test only (we can not compensate cost of ultrasound) and will be processed in a few business days.
There is no reimbursement for inconclusive fetal sex results. In those rare cases we will offer you anatomy and gender scan for reduced cost and will discuss the findings and need for further referrals.
There is usually no need to delay your NIPT until after the NHS nuchal translucency (NT) scan at 12–14 weeks. NIPT can be carried out from as early as 9–10 weeks, and having it sooner means you are reassured about Down’s, Edwards’ and Patau’s syndromes earlier in your pregnancy. NIPT is a more accurate screening test for these conditions than the Combined Test, so most parents choose not to wait.
At London Pregnancy Clinic we recommend NIPT alongside our 10 Week Scan, which checks your baby’s early development and confirms dates for the laboratory. Having both together at around 10 weeks leaves plenty of time for a redraw if needed, or for a referral should anything unexpected be found. We still encourage you to attend your NHS appointments for continuity of care. If you are unsure about timing, our specialists can advise at a viability scan.
Vanishing twin is a situation with twin pregnancies when the embryo or fetus in one of the sacs fails to develop or dies at the early stages of pregnancy. Interpretation of NIPT in the case of vanishing twin phenomenon is complicated due to contamination of the sample by DNA of non developing twin pregnancy. Both Harmony and Panorama NIPT cannot be used this situation.
However we have specific solution for pregnancies affected by this rare condition: we have Invitae NIPS, which can be used in the cases of vanishing twin phenomenon. Please get in touch to enquire.
Yes. Through Jeen Health, you can access the Panorama NIPT test anywhere in the UK.
Jeen’s specialists review your scan to confirm suitability, followed by a 20-minute consultation with a genetic counsellor to help choose the right test.
Blood samples can be collected locally, at our London clinics, or with a home phlebotomy service (+£65). Test kits are shipped by next-day delivery, with results securely online.
Panorama Microdeletions NIPT is also available across the UK, including Manchester, Liverpool and Edinburgh.
Not through London Pregnancy Clinic — every NIPT we offer includes an expert ultrasound scan. The scan confirms your pregnancy is viable, dates it accurately and checks it is suitable for testing, which is why we do not offer the blood test on its own.
If you cannot get to our London clinic, our partner Jeen Health offers NIPT across the UK, including Panorama. You will need to provide proof of a pregnancy scan taken within the last 7 days before your blood sample is taken.
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