FISH Test Menu
LIST OF FLUORESCENCE IN SITU HYBRIDIZATION PROBES – HEMATOLOGICAL MALIGNANCIES
ACUTE MYELOGENOUS LEUKEMIA (AML) / MYELODYSPLASTIC SYNDROME (MDS) PANEL*
5q deletion / monosomy 5 TAS2R1 / EGR1
t(8;21) ETO / AML1
t(15;17) PML / RARA
inv(16) MYH11 / CBFB
17p deletion p53
20q deletion / monosomy 20 MYBL2 / PTPRT
7q deletion / monosomy 7 RELN / TES
11q rearrangement MLL
ACUTE LYMPHOCYTIC LEUKEMIA (ALL) PANEL (B-cell)*
8q rearrangement cMYC
9p deletion p16 / D9Z3
hyperdiploidy – chr. 4 FIP1L1 / CHIC2 / PDGFRA
hyperdiploidy – chrs. 10 & 17 D10Z1 / D17Z1
t(12;21) ETV6 / AML1
11q rearrangement MLL
t(9;22) ABL1 / BCR
14q rearrangement IGH
CHRONIC LYMPHOCYTIC LEUKEMIA (CLL) PANEL*
6q deletion D6Z1 / MYB
trisomy 12 D12Z1
11q deletion D11Z1 / ATM
t(14;18) IGH / BCL2
14q rearrangement IGH
17p deletion p53
t(11;14) CCND1 / IGH
13q deletion RB1 / CTB-163C9
MULTIPLE MYELOMA (MM) PANEL (on isolated plasma cells)*
11q deletion D11Z1 / ATM
17p deletion p53
13q deletion RB1 / CTB-163C9
t(11;14) CCND1 / IGH
t(4;14) FGFR3 / IGH
t(14;16) IGH / MAF
hyperdiploidy ATM / MAF / FGFR3
MYELOPROLIFERATIVE DISEASE (MPD) PANEL*
t(9;22) ABL1 / BCR
4q rearrangement FIP1L1 / CHIC2 / PDGFRA
T(5;12) PDGFRB
8p11 rearrangement FGFR1
T-CELL LYMPHOMA PANEL*
inv(7) / iso(7q) TCRB
inv(14) / 14q rearrangement TCRAD
t(2;5) / 2p rearrangement ALK
B-CELL LYMPHOMA PANEL*
t(14;18) IGH / BCL2
8q rearrangement cMYC
3q rearrangement BCL6
OTHER FISH TESTS
*Any of the probes listed under panels can be ordered as single FISH tests in addition to the probes listed below.
t(9;22) ABL1 / BCR
t(11;22) EWSR1
LIST OF FLUORESCENCE IN SITU HYBRIDIZATION PROBES – CONSTITUTIONAL ABNORMALITIES
ANEUVYSION (Amniotic Fluid)
13 / 21 RB1 / D21S259,D21S341,D21S342
18 / X / Y D18Z1 / DXZ1 / DYZ3
PRODUCTS OF CONCEPTION (POC)
13 / 21 RB1 / D21S259,D21S341,D21S342
18 / X / Y D18Z1 / DXZ1 / DYZ3
16 D16Z2
MICRODELETION PROBES
22q11 deletion (DiGeorge / VCFS syndrome) HIRA / TUPLE1
15q11 deletion (Prader-Willi syndrome) SNRPN / 154P1
15q11 deletion (Angelman syndrome) UBE3A / 154P1
Yp deletion SRY / DXZ1
LIST OF FLUORESCENCE IN SITU HYBRIDIZATION PROBES – CONSTITUTIONAL ABNORMALITIES
ANEUVYSION (Amniotic Fluid)
13 / 21 RB1 / D21S259,D21S341,D21S342
18 / X / Y D18Z1 / DXZ1 / DYZ3
PRODUCTS OF CONCEPTION (POC)
13 / 21 RB1 / D21S259,D21S341,D21S342
18 / X / Y D18Z1 / DXZ1 / DYZ3
16 D16Z2
MICRODELETION PROBES
22q11 deletion (DiGeorge / VCFS syndrome) HIRA / TUPLE1
15q11 deletion (Prader-Willi syndrome) SNRPN / 154P1
15q11 deletion (Angelman syndrome) UBE3A / 154P1
Yp deletion SRY / DXZ1