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Choose a Chromosome

Key

H Haematology
S Solid tumour
C Cytogenetics & rare disease

Chromosome

11.3211.3111.2111.231211.22111.211.22211.22311.111.1
Regions Probe
Xp22.33 / Yp11.32 H CytoCell CRLF2 Breakapart View
Xp11.1-q11.1 / Yp11.1-q11.1 / Yq12 C CytoCell Dual Labelled Satellite Probe Sets View
18p11.1-q11.1 (D18Z1) / Xp11.1-q11.1 (DXZ1) / Yp11.1-q11.1 (DYZ3) C CytoCell FAST FISH Prenatal X, Y and 18 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
Xp22.33 / Yp11.32 H CytoCell P2RY8 Deletion View
18p11.1-q11.1 (D18Z1) / Xp11.1-q11.1 (DXZ1) / Yp11.1-q11.1 (DYZ3) C CytoCell Prenatal X, Y and 18 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
Xp22.33 / Xp11.1-q11.1 / Yp11.32 / Yq12 / Xp11.1 C CytoCell SHOX View
Yp11.31 / Yq12 C CytoCell SRY View
1-22, X, Y C CytoCell Subtelomere Specific Probes View
1-22, X, Y C CytoCell TeloMark Kit View