Claritest NIPT with 22q11.2 Deletion ClariNIPTM

Synonyms

Allscripts (AEHR) Order Name

ClariTest NIPT w/ Microdeletions

Sunrise Clinical Manager (SCM) Order Name

Clari Test NIPT w/microdeletions

Clinical Info

Prenatal screening test for Down syndrome, trisomy 18, trisomy 13, sex chromosome abnormalities, and 22q11.2 microdeletion syndrome

Specimen Type

Container

Cell-Free DNA BCT Streck

Collection Instructions

Container/Tube: Cell-free DNA White Top Roche Tube
Specimen: 2 Roche tubes whole Blood
Transport Temperature: Room Temperature
Stability: 5 Days

If the sex chromosomes option is selected, results for Monosomy X, XXX, XXY and XYY
will be included.
Test requires the following information for testing
1) Estimated Due Date (EDD)
2) Pregnancy Type (Single, Twin)
3) Is gender required on report (Yes/No)

Transport Instructions

Room Temperature

Specimen Stability

5 Days

If the sex chromosomes option is selected, results for Monosomy X, XXX, XXY and XYY
will be included.
Test requires the following information for testing
1) Estimated Due Date (EDD)
2) Pregnancy Type (Single, Twin)
3) Is gender required on

Methodology

cfDNA is sequenced using microarray quantitation and DANSR and the FORTE algorithm.

Days Performed

Performing Laboratory

BioReference Laboratories
Prenatal screening test for Down syndrome, trisomy 18, trisomy 13, sex chromosome abnormalities, and 22q11.2 microdeletion syndrome

CPT

81507
81422


Turnaround Time:
6-8 days

PDM

1759834

Result Interpretation

Results for chromosomes 21, 18, 13 and sex chromosomes are reported as:
• No Aneuploidy Detected
• Aneuploidy Detected
• Aneuploidy Suspected – Borderline Value (reported for chromosomes 21, 18 and 13 only)
Plus
Results for microdeletions are reported as:
• No Microdeletions Detected
• Abnormality Detected

Forms

• Prenatal Genetics Requisition