NIPT Comprehensive – Trisomy, Sex Chromosome, RAA & CNV

A broader non-invasive prenatal screen for singleton pregnancies, adding rare autosomal aneuploidy and large copy-number variation screening to the named trisomies and fetal chromosomal sex information. This is screening, not a diagnosis; discuss results with your clinician.

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AED 1,690
Sample
Maternal blood
Expected results
7–12 days
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Processed by a CAP-accredited partner laboratory: Al Moosa Diagnostic Center / MDC Labs.

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About this test

A broader non-invasive prenatal screen for singleton pregnancies, adding rare autosomal aneuploidy and large copy-number variation screening to the named trisomies and fetal chromosomal sex information. This is screening, not a diagnosis; discuss results with your clinician.

What's included

  • Screening for trisomies 13, 18 and 21
  • Rare autosomal aneuploidy (RAA) screening
  • Fetal chromosomal sex information
  • Large copy-number variation (CNV) screening for changes greater than 7 Mb

Quick facts

  • Test type: Comprehensive non-invasive prenatal screening
  • Pregnancy type: Singleton, as specified by the catalogue
  • Sample: Maternal blood
  • Results: 7–12 days, with a maximum turnaround of 12 days
  • Interpretation: Screening only; confirmatory assessment may be recommended

Results and included services

Expected results

7–12 days

Questions about this test

What does Comprehensive NIPT assess? The catalogue lists trisomies 13, 18 and 21, rare autosomal aneuploidies, fetal chromosomal sex and large copy-number variations over 7 Mb.

Is this package listed for twins? The catalogue describes this particular comprehensive option for singleton pregnancies; ask the clinic about twin pregnancy options.

What sample is needed? A maternal blood sample is listed.

When will results be ready? Results are available in 7–12 days, with a maximum turnaround of 12 days.

Does this test diagnose a chromosomal condition? No. It is a screening test, and a clinician may recommend confirmatory testing.

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