Chromosomal Microarray, pregnancy loss
Collection Requirements
Source: fetal tissue
Container: sterile cup or tube with sterile
transport medium
Volume: 1-2 cm3
Source: maternal blood
Container: EDTA lavender
Volume:
- Preferred: 3 mL in vacutainer
- Minimum: 1 mL in vacutainer
Special Instructions
- Transport at room temperature; avoid fluctuating temperatures (hot or cold)
- Specimen must be processed within 24 hours of collection
- Contact Genetics for collection materials
- Use the Prenatal and Pregnancy Loss Cytogenetics Requisition
Turn Around Time
21 days
Availability
Routine
Lab Processing Instructions
Specimen: whole blood
Room temperature
Performing Laboratory
Genetics
Adele Hall Lab Section
Cytogenetics
Instrumentation/Methodology
Microarray
Additional Information
Advantages: Evaluates hundreds of different genetic conditions, including aneuploidy. Detects large and small deletions and duplications, which may not be detected by conventional chromosome analysis. Detects regions of homozygosity. DNA isolated from fresh tissue. Limitations: Cannot identify truly balanced chromosomal aberrations, i.e., balanced translocations, inversion, insertions, etc. Cannot detect point mutations or epigenetic changes. Cannot detect genomic imbalances in regions not represented on the microarray. Low-level mosaicism may not be detected.
Reference Ranges
See interpretive report
CPT
81229