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Test Code POCMY / 110-AD Microarray Products of Conception

Important Note

This test may require pre-authorization or have limited coverage.  Please check with your appropriate insurance carrier to determine any specific requirements.

Additional Codes

Software                                    Test Code                                      
SoftID  POCMY
EPIC LAB20422
Allele Diagnostics 110

Performing Laboratory

Allele Diagnostics

Useful For

Microarray is useful for detecting most large and small structural chromosome abnormalities and copy neutral AOH with rapid results.

The CGH portion of this microarray can identify numeric chromosomal abnormalitiesas well as unbalanced structural abnormalities. The microarray is designed to target pericentromericregions, subtelomeric regions, and regions associated with copy number abnormalities.

The SNP component of this microarray will detect long continuous stretches ofhomozygosity (or absence of heterozygosity, AOH).

Method Name

Microarray CGH with SNP analysis

Report Available

2-4 Days

Specimen Type

Products of Conception in Sterile Media (Preferred) or Sterile Saline – Sterile RPMI media is preferred.

Preferred Container

Sterile IATA-Approved Screw-Capped Plastic Container

Preferred Volume

Products of Conception in Sterile Media (Preferred) or Sterile Saline: 20 mg (Sterile IATA-Approved Screw-Capped Plastic Container)

Minimum Volume

Products of Conception in Sterile Media (Preferred) or Sterile Saline: 5 mg (Sterile IATA-Approved Screw-Capped Plastic Container)

Specimen Collection and Handling

Specimens should be shipped at room temperature in a leak-proof, rigid container with overnight delivery.

Add On Capable

Not Permitted

CPT Code Information

CPT Code

CPT Description

CPT Disclaimer
81229 Cytogenomic (genome-wide) microarray analysis  
88235 Tissue Culture, Placenta  
88283 Chromosome banding study  

Keywords

POC

CGH with SNP analysis

Clinical Significance

Abnormal fetal ultrasound.

Diagnosis of trisomies in addition to microdeletions/duplications for rapid results.

Family history of balanced rearrangement (for detection of unbalanced rearrangement).

Fetal loss or stillbirth.

LOINC Code Information

86611-1