Cytocell Hero

Choose a Chromosome

Key

H Haematology
S Solid tumour
C Cytogenetics & rare disease

Chromosome

131211.211.22122.122.222.311.111.1
Regions Probe
13p13 / 14p13 / 15p13 / 21p13 / 22p13 C CytoCell Acro-P-Arm Probe View
21q22.12 H CytoCell AML1 (RUNX1) Breakapart View
21q22.12 / 8q21.3 H CytoCell AML1/ETO (RUNX1/RUNX1T1) Translocation, Dual Fusion View
22q12.1-q12.2 / 21q22.13-q22.2 S CytoCell EWSR1/ERG Translocation, Dual Fusion View
13q14.2 / 21q22.13 C CytoCell FAST FISH Prenatal 13 and 21 View
13q14.2 / 18p11.1-q11.1 (D18Z1) / 21q22.13 / Xp11.1-q11.1 (DXZ1) / Yp11.1-q11.1 (DYZ3) C CytoCell FAST FISH Prenatal X, Y, 13, 18 and 21 View
13q14.2 / 21q22.13 C CytoCell Prenatal 13 and 21 View
13q14.2 / 18p11.1-q11.1 / 21q22.13 C CytoCell Prenatal 13, 18 and 21 View
13q14.2 / 18p11.1-q11.1 (D18Z1) / 21q22.13 / Xp11.1-q11.1 (DXZ1) / Yp11.1-q11.1 (DYZ3) C CytoCell Prenatal X, Y, 13, 18 and 21 View
1-22, X, Y (centromere) C CytoCell Satellite Enumeration Probes View
1-22, X, Y C CytoCell Subtelomere Specific Probes View
12p13.2 / 21q22.12 H CytoCell TEL/AML1 (ETV6/RUNX1) Translocation, Dual Fusion View
1-22, X, Y C CytoCell TeloMark Kit View
21q22.2-q22.3 / 21q22.13-q22.2 S CytoCell TMPRSS2/ERG Deletion/Breakapart View