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Chromosome Analysis, Blood
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Test Name: Chromosome Analysis, Blood
Reference Lab: QNI
Test Code: 14596
Shipping Temp: Room temperature
Specimen Type: 5 mL whole blood collected in a sodium heparin (green-top) tube
TAT: 10-12 days
CPT Code: 88230, 88262
Cost:
Additional Comments: _
FDA Approved Test: YES_ NO_ LDT_
Medical Director/Pathologist: approved by
Billing Completed by_ Date_ Time_
Test Name: Chromosome Analysis, Blood
Reference Lab: QNI
Test Code: 14596
Shipping Temp: Room temperature
Specimen Type: 5 mL whole blood collected in a sodium heparin (green-top) tube
TAT: 10-12 days
CPT Code: 88230, 88262
Cost:
Additional Comments: _
FDA Approved Test: YES_ NO_ LDT_
Medical Director/Pathologist: approved by
Billing Completed by_ Date_ Time_
Test Code
PESOT/Chromosome Analysis, Blood
Quest Code
14596
Alias/See Also
QNI Flexi 14596
CPT Codes
88230, 88262
Physician Attestation of Informed Consent
This genetic test requires provider confirmation that patient informed consent has been received if the ordering provider is located in AK, AZ, DE, FL, GA, IA, MA, MN, MT, NV, NH, NJ, NY, OR, SC, SD, or VT or testing is performed in MA.
Includes
**Test may be replaced by %37871 Chromosome Analysis, Blood, No Growth and %39650 Cytogenetics Communication**
Preferred Specimen
5 mL whole blood collected in a sodium heparin (green-top) tube
Minimum Volume
1 mL • Critical NICU/Neonates 0.5 mL
Other Acceptable Specimens
Sodium heparin (royal blue-top) tube • Sodium heparin lead-free (tan-top) tube
Instructions
Other vacutainer tubes containing sodium heparin are acceptable. See Genetics Specimen Collection Section for detailed specimen instructions.
Transport Temperature
Room temperature
Specimen Stability
Room temperature: Preferred
Refrigerated: Acceptable
Frozen: Unacceptable
Specimen viability decreases during transit. Send specimen to testing lab for viability determination. Do not freeze. Do not reject.
Refrigerated: Acceptable
Frozen: Unacceptable
Specimen viability decreases during transit. Send specimen to testing lab for viability determination. Do not freeze. Do not reject.
Methodology
Culture • Karyotype • Microscopy
FDA Status
This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.
Setup Schedule
Set up: Daily; Report available: 10 days
Reference Range
See Laboratory Report
Clinical Significance
This test may assist with the detection of common chromosome abnormalities.
Performing Laboratory
Quest Diagnostics Nichols Institute
33608 Ortega Highway
San Juan Capistrano, CA 92675-2042

