Epic Code LAB2111365 Chronic Lymphocytic Lymphoma (CLL) Probe Panel by FISH
Test Name Alias
Chronic Lymphocytic Lymphoma (CLL) Probe Panel by FISH | 992
Interface Order Alias
11379
Quick Collect
AP Ambient
Clinical Information
This probe panel detects specific numerical and structural chromosome abnormalities commonly associated with CLL.
Routine chromosome analysis is performed on all bone marrow specimens and is recommended on all diagnostic samples to exclude abnormalities not identified by the specified FISH probe(s).
Panel Information
Panel testing includes:
- 11q-, ATM
- 17p-, TP53
- 13q-, D13S319+
- +12, D12Z3
- t(11;14), IGH@/CCND1
Collection Instructions
Multiple specimen collection types. Submit only one:
Specimen Collection: Bone Marrow
Container(s): Green Top (Sodium Heparin)
Preferred volume to collect: 5.0 mL
Minimum volume to collect: 1.0 mL
Neonate volume to collect: 1.0 mL
Collection Instructions:
- Collect bone marrow and transfer marrow from syringe to plain green top sodium heparin tube.
Specimen Collection: Peripheral blood
Container/Tube: Green Top (Sodium Heparin)
Preferred volume to collect: 8.0 mL
Minimum volume to collect: 0.5 mL
Neonate volume to collect: 0.5 mL
Collection Instructions:
- Collect peripheral blood into a plain green top sodium heparin tube.
- Keep sample at room temperature and send to the Lab immediately.
Processing Instructions (Laboratory, Outpatient or Off-site collection)
Spin: N
Aliquot: N
Transport Temperature: Ambient
If ambient temperature exceeds 80°F or is below 40°F, please send in an insulated container. All samples should be directed to the laboratory as soon as possible.
Specimen Stability
Ambient: 3 days (beyond 3 days, specimen viability will be detemined by Cytogenetics Lab)
Laboratory Retention: primary specimens 4 weeks; frozen pellets retained greater than 1 year
Test Frequency
Test Set Up: Monday – Friday 8:00 am – 5:00 pm, Saturday 8:00 am – 3:00 pm.
Technologist on call for Sunday set up.
Final report: 2 – 3 days.
Reference Range
An interpretative report will be provided.
Performing Department
Cytogenetics
Performing Department Laboratory Location
Corewell Health Advanced Technology Laboratory (ATL), Grand Rapids, MI
Methodology
Performed by Fluorescence In-Situ Hybridization (FISH). This test was developed and its performance characteristics determined by Spectrum Health Cytogenetics. It has not been cleared or approved by the U.S. FDA. The FDA has determined that such clearance or approval is not necessary. This test is used for clinical purposes.
CPT
88271 x5, 88275 x8
CDM Code
3108827102, 3108827501
Epic Test ID
1230100491
LOINC
Specimen Type: 66746-9
Indication Provided: 42349-1
Result: in process
Interpretation: 59050-5
Comments: 69965-2
Reviewed Date
4/28/2023