SNP Microarray−Products of Conception (POC)/Tissue (Reveal®)

CPT: 81229
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Synonyms

  • Reveal® SNP Microarray−Products of Conception (POC)/Tissue

Special Instructions

Pertinent medical findings must accompany test request form. For formalin fixed paraffin embedded blocks or slides, test number will be updated to Microarray-Products of Conception (POC) Reveal® FFPE [511997]. If <8 mg nonfixed tissue is received, sample will be assessed to run on the Oncoscan Microarray platform, and test number adjusted as necessary and client notified.

If prior NIPT studies have been performed, include copy of the report.


Expected Turnaround Time

12 - 18 days




Specimen Requirements


Specimen

Preferred nonfixed tissue or products of conception (POC)/placental villus biopsy


Volume

>8 mg tissue


Container

Sterile container containing sterile Ringer's lactate or Hanks' balanced salt solution or transport medium provided by the cytogenetics laboratory. (Do not use isotonic saline as a transport medium or urine containers for shipping.) Specialized kits are now available for POC microarray testing. To order, please contact your local Labcorp representative. PeopleSoft: 89063, Catalogue No. 39025G.


Collection

Aseptically obtain a small piece of fetal tissue that does not appear necrotic. If specimen is a POC, placental villi or membranes may be the only fetal-derived tissue available, and an effort should be made to submit these tissues rather than maternal decidua.


Storage Instructions

Maintain specimen at room temperature.


Causes for Rejection

Quantity not sufficient for analysis; necrotic tissue submitted


Test Details


Use

This test will detect chromosomal imbalance that could be associated with developmental delay/congenital anomalies. It provides possible detection of uniparental disomy of any chromosome, the percent and location of homozygosity, including the degree of identity by descent. It will also allow the detection of complete or partial molar pregnancies.


Limitations

Unable to determine genotypes on some formalin-fixed tissue (blocks/slides), allowing only genomic dosage to be determined. This SNP assay does not detect balanced rearrangements, low-level mosaicism (<10%), marker chromosomes that only contain heterochromatin or tetraploidy.

This test was developed and its performance characteristics determined by Labcorp. It has not been cleared or approved by the Food and Drug Administration.


Methodology

SNP microarray analysis is performed using the Cytoscan® HD Accel platform, which uses 743,130 SNP probes and 2,029,441 NPCN probes with a median spacing of 0.818 kb.


Additional Information

The microarray will detect DNA copy-number changes at a threshold >1 Mb for deletions, >2 Mb for duplications.


References

Coppinger J, Alliman S, Lamb A, et al. Whole-genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarray. Prenatal Diagn. 2009 Dec; 29(12):1156-1166.19795450

LOINC® Map

Order Code Order Code Name Order Loinc Result Code Result Code Name UofM Result LOINC
510110 POC/Tissue Microarray 510112 Specimen Type 31208-2
510110 POC/Tissue Microarray 510113 # of Genotyping Targets N/A
510110 POC/Tissue Microarray 510114 Array Type N/A
510110 POC/Tissue Microarray 510116 Diagnosis 48000-4
510110 POC/Tissue Microarray 510117 Interpretation 62365-2
510110 POC/Tissue Microarray 510118 Director Review: 48672-0
510110 POC/Tissue Microarray 512123 PDF 51967-8

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