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Choose a Chromosome

Key

H Haematology
S Solid tumour
C Cytogenetics & rare disease

Chromosome

13.313.313.413.213.213.113.112121111
Regions Probe
1p36.32 / 1q25.2 / 19p13.2 / 19q13.33 S CytoCell 1p36/1q25 and 19q13/19p13 Deletion Probe Kit View
19p13.3 H CytoCell E2A (TCF3) Breakapart View
1q23.3 / 17q22 / 19p13.3 H CytoCell E2A (TCF3)/PBX1 Plus Translocation, Dual Fusion Probe View
1q23.3 / 19p13.3 H CytoCell E2A (TCF3)/PBX1 Translocation, Dual Fusion View
11q23.3 / 19p13.3 H CytoCell MLL (KMT2A)/MLLT1 Translocation, Dual Fusion View
4q12 / 8q24.21 / 9p21.3 / 9q34.11-q34.12 / 9q12 / 11q23.3 / 12p13.2 / 14q32.33 / 19p13.3 / 21q22.12 / 22q11.22-q11.23 H CytoCell Multiprobe ALL Panel v2 (RUO) View
1-22, X, Y (centromere) C CytoCell Satellite Enumeration Probes View
1-22, X, Y C CytoCell Subtelomere Specific Probes View
1-22, X, Y C CytoCell TeloMark Kit View