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26329 ClariTest Core NIPS with del 22q

ClariTest Core NIPS with del 22q
Test Code: CLAR2SO
Synonyms/Keywords

​Trisomy 21 (Down Syndrome), Trisomy 18 (Edward syndrome), Trisomy 13 (Patau syndrome), Monosomy X (Turner syndrome), XXY (Klinefelfter syndrome), XXX (Trisomy X), XYY (Jacob syndrome), XXYY, Other sex aneuploidies, 22q11.2 microdeletion syndrome also known as DiGeorge syndrome

Useful For

​Conditions screened for with Core NIPS: Tryisomy 21 (Down Syndrome), Trisomy 18 (Edward syndrome), Trisomy 13 (Patau syndrome), Monosomy X (Turner syndrome), XXY (Klinefelfter syndrome), XXX (Trisomy X), XYY (Jacob syndrome), XXYY, Other sex aneuploidies, 22q11.2 microdeletion syndrome also known as DiGeorge syndrome

Specimen Requirements
Fasting RequiredSpecimen TypePreferred Container/TubeAcceptable Container/TubeSpecimen VolumeSpecimen Minimum Volume
(allows for 1 repeat)		Pediatric Minimum Volume
(no repeat)
​No​Whole Blood​Kit test with two Cell-Free DNA White Top plastic tubes.​​10 mL​7 mL​
Collection Processing Instructions

​Collect blood according to the instructions provided in the kit.

Required fields to be filled out on the Req.: Patient demographic and insurance info, appropriate diagnosis codes, pregnancy type (singleton, twin), IVF pregnacy (Y/N): if yes, donor egg {self/non-self} and age of egg at retrieval, estimated due date, maternal weight.

MUST store at room temperature.  Send ambient.

Specimen Stability Information
Specimen TypeTemperatureTime
​Whole Blood​Ambient​7 days
Performing Laboratory Information
Performing LocationDay(s) Test PerformedAnalytical TimeMethodology/Instrumentation
​GenPath BioReference Laboratories​Sunday through Saturday​5-7 days​Microarray quantitation with DANSR assay and FORTE algorithm
Reference Lab
GenPath BioReference Laboratories
Synonyms/Keywords

​Trisomy 21 (Down Syndrome), Trisomy 18 (Edward syndrome), Trisomy 13 (Patau syndrome), Monosomy X (Turner syndrome), XXY (Klinefelfter syndrome), XXX (Trisomy X), XYY (Jacob syndrome), XXYY, Other sex aneuploidies, 22q11.2 microdeletion syndrome also known as DiGeorge syndrome

Ordering Applications
Ordering ApplicationDescription
​Cerner​ClariTest Core NIPS with del 22q
If the ordering application you are looking for is not listed, contact your local laboratory for assistance.
Specimen Requirements
Fasting RequiredSpecimen TypePreferred Container/TubeAcceptable Container/TubeSpecimen VolumeSpecimen Minimum Volume
(allows for 1 repeat)		Pediatric Minimum Volume
(no repeat)
​No​Whole Blood​Kit test with two Cell-Free DNA White Top plastic tubes.​​10 mL​7 mL​
Collection Processing

​Collect blood according to the instructions provided in the kit.

Required fields to be filled out on the Req.: Patient demographic and insurance info, appropriate diagnosis codes, pregnancy type (singleton, twin), IVF pregnacy (Y/N): if yes, donor egg {self/non-self} and age of egg at retrieval, estimated due date, maternal weight.

MUST store at room temperature.  Send ambient.

Specimen Stability Information
Specimen TypeTemperatureTime
​Whole Blood​Ambient​7 days
Useful For

​Conditions screened for with Core NIPS: Tryisomy 21 (Down Syndrome), Trisomy 18 (Edward syndrome), Trisomy 13 (Patau syndrome), Monosomy X (Turner syndrome), XXY (Klinefelfter syndrome), XXX (Trisomy X), XYY (Jacob syndrome), XXYY, Other sex aneuploidies, 22q11.2 microdeletion syndrome also known as DiGeorge syndrome

For more information visit:
Performing Laboratory Information
Performing LocationDay(s) Test PerformedAnalytical TimeMethodology/Instrumentation
​GenPath BioReference Laboratories​Sunday through Saturday​5-7 days​Microarray quantitation with DANSR assay and FORTE algorithm
Reference Lab
GenPath BioReference Laboratories
For billing questions, see Contacts
For most current information refer to the Marshfield Laboratory online reference manual.