CHROMOSOMAL MICROARRAY PRENATAL

This prenatal chromosomal microarray test screens for genetic abnormalities in the fetus, such as chromosomal deletions or duplications. It is often recommended for high-risk pregnancies to detect conditions like Down syndrome and other genetic disorders.

Also known asChromosomal Microarray - Prenatal Chromosomal Microarray - Prenatal

Available via

Home Collection, Lab Visit

Contains

7 parameters

Earliest reports in

15 Working Days

Test details
Preparations

No special preparations needed

Test included
CHROMOSOMAL MICROARRAY PRENATAL includes 7 parameters

  • Specimen
  • Clinical History

  • Deletion
  • Duplication
  • Autosomal Aneuploides
  • Sex Chromosome Aneuploidy
  • Interpretation

Test code

6042M

Specimen vol. and vacutainer information
SpecimenVacutainerVolume
Amniotic FluidPlain Sterile Vaccutainer 2 ML
Chorionic VillusOthers2 ML
Others (fx)Others2 ML

Specimen stability information

Amniotic Fluid, Chorionic Villus, Others (Fx), Others (Fx)

Collection instructions

Age,Gender,Clinical history required

Specimen rejection criteria

Test run frequency

'

Turn around time

15 Working Days

Performing locations

Department

  • Cytogenetics

CPT and Loinc codes

CHROMOSOMAL MICROARRAY PRENATAL

16500