FISH Interphase
Ordering Recommendation
Use to order individual or multiple oncology FISH probes if standard FISH panels are not desired. Refer to the listing of oncology FISH probes at https://www.aruplab.com/genetics/tests/fish-oncology.
New York DOH Approval Status
Specimen Required
Nondiluted bone marrow aspirate collected in a heparinized syringe.
Also acceptable: Bone marrow or whole blood collected in green (sodium heparin).
Transfer 3 mL bone marrow to a green (sodium heparin) (Min: 1 mL) OR transport 5 mL whole blood (Min: 2 mL)
Preferred transport temp: Room temperature.
Paraffin-embedded specimens. Clotted specimens.
Desired FISH probe(s), specimen type, and pertinent clinical diagnosis are required with test order. Testing will not be performed until probe(s), specimen type, and diagnosis are provided; absence of this information will delay turnaround time.
Ambient: 2 days; Refrigerated: 2 days; Frozen: Unacceptable
Methodology
Fluorescence in situ Hybridization (FISH)
Performed
Sun-Sat
Reported
3-9 days
Reference Interval
Interpretive Data
Laboratory Developed Test (LDT)
Note
Time required for testing can vary depending on specimen type and probes ordered.
Please indicate the names of probes needed for testing and specimen type. Refer to Ordering Recommendations for a link to available FISH probes.
Contact ARUP Genetics Service Support at extension 3301 to add a probe to a current specimen.
If more than one FISH probe is ordered, additional probe and analysis charges will be applied per probe.
Other specimen types may be acceptable, contact ARUP Genetics Support Services at extension 3301 for specific specimen collection and transportation instructions.
If chromosome analysis is not performed at ARUP on the same sample, Bone Marrow/PBL Culture Processing Fee (0093271) will be added to account for sample processing, and an additional charge will apply. If multiple FISH tests are ordered, 0093271 will only be applied to one of the FISH tests. If cell pellets or dropped cytogenetic slides are submitted, processing fee will not apply.
This test must be ordered using Oncology test request form #43099 or through your ARUP interface.
Hotline History
Hotline History
CPT Codes
88271; 88275
Components
| Component Test Code* | Component Chart Name | LOINC |
|---|---|---|
| 3020330 | EER FISH Interphase | 11526-1 |
| 3020331 | FISH Interphase | 57802-1 |
Aliases
- 1p32 (CDKN2C), 1p Loss/Deletion, CDKN2C/CKS1B (1p/1q)
- 1q21 (CKS1B), 1q Gain/Amplification, with 1p32 (CDKN2C)
- 1q25 (ABL2) Breakapart, ABL2 Rearrangement
- GATA2::MECOM (RPN1-EVI1) Fusion, inv(3)(q21q26.2), t(3;3)(q21;q26.2), inv(3)/t(3;3)
- 3q26 (MECOM) Breakapart, MECOM (EVI1) Rearrangement (non-NY approved)
- 3q27 (BCL6) Breakapart, BCL6 Rearrangement
- +4, Trisomy 4, Hyperdiploidy
- IGH::FGFR3 Fusion, t(4;14)(p16;q32)
- 4q12 FIP1L1::PDGFRA Fusion, PDGFR-alpha/PDGFRA Rearrangement, PDGFRA-CHIC2-FIP1L1 with CHIC2 Deletion
- 5q31 (EGR1) Deletion, Loss/Deletion 5q, del(5q), -5, Monosomy 5, with 5p15 (D5S23)
- 5q32 (CSF1R) Breakapart, CSF1R Rearrangement
- 5q32 (PDGFRB) Breakapart, PDGFR-beta/PDGFRB Rearrangement
- 7p12 IKZF1 (IKAROS) Deletion, Loss/Deletion 7p, del(7p)
- 7q31 (D7S486) Deletion, Loss/Deletion 7q, del(7q), -7, Monosomy 7
- +8, Trisomy 8
- 8p11.2 (FGFR1) Breakapart, FGFR1 Rearrangement
- RUNX1T1::RUNX1 (ETO::AML1) Fusion, t(8;21)(q22;q22), iAMP21, +8, +21
- 8q24 (MYC) Breakapart, MYC rearrangement
- IGH::MYC Fusion/Rearrangement, t(8;14)(q24;q32)
- +9, Trisomy 9, Hyperdiploidy
- 9p24 (JAK2) Breakapart, JAK2 Rearrangement, +9, Trisomy 9, Hyperdiploidy
- 9p21 (CDKN2A) Deletion, Loss/Deletion 9p, del(9p)
- 9q34 (ABL1) Breakapart, ABL1 Rearrangement
- BCR::ABL1 Fusion, Philadelphia (Ph) chromosome, t(9;22)(q34;q11.2)
- +10, Trisomy 10, Hyperdiploidy
- IGH::CCND1 Fusion/Rearrangement, t(11;14)(q13;q32), +11
- 11p15 (NUP98) Breakapart, NUP98 Rearrangement
- 11q22 (ATM) deletion, Loss/Deletion 11q, del(11q)
- 11q23 (KMT2A) Breakapart, KMT2A (MLL) Rearrangement, Loss/Deletion 11q, del(11q)
- +12, Trisomy 12
- 12p13 (ETV6) Breakapart, ETV6 Rearrangement, Loss/Deletion 12p, del(12p)
- ETV6::RUNX1 (TEL-AML1) Fusion, t(12;21)(p13;q22), iAMP21, Loss/Deletion 12p, del(12p), +21
- 13q14 (D13S319) Deletion, Loss/Deletion 13q, with 13q34 (LAMP1)
- 14q32 (TCL1A) Breakapart, TCL1A Rearrangement
- 14q32 (IGH) Breakapart, IGH Rearrangement
- IGH::MAF Fusion/Rearrangement, t(14;16)(q32;q23)
- IGH::BCL2 Fusion/Rearrangement, t(14;18)(q32;q21)
- IGH::MAFB Fusion/Rearrangement, t(14;20)(q32;q12)
- PML::RARA Fusion, t(15;17)(q24;q21), +15, +15q, +17, +17q
- 16q22 (CBFB) Breakapart, CBFB Rearrangement
- CBFB::MYH11 Fusion, t(16;16)(p13.1;q22), inv(16)(p13.3q22), inv(16)/t(16;16)
- +17, Trisomy 17, Hyperdiploidy
- del(17)(p13.1) (TP53) Deletion, TP53 (p53) Deletion
- 18q21 (MALT) Breakapart, MALT1 Rearrangement
- 19p13.3 (TCF3) Breakapart, TCF3 (E2A) Rearrangement
- 19p13.2 (EPOR) Breakapart, EPOR Rearrangement
- 20q12 (D20S108) Deletion, Loss/Deletion 20q, del(20q), with 20q13 (MYBL2)
- 21q22 (RUNX1) Breakapart, RUNX1 Rearrangement, iAMP21, +21
- 21q22 (RUNX1) amp, with 12p13 (ETV6), iAMP21
- 22q12 (EWSR1) Breakapart, EWSR1 Rearrangement
- Xp22/Yp11 (CRLF2) Breakapart/Deletion, CRLF2 Rearrangement, CRLF2 5' Deletion/P2RY8::CRLF2 Fusion
- X and Y centromere (CEP X/Y), DXZ1, DYZ3
















