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Fig. 2 | Molecular Cytogenetics

Fig. 2

From: Monoallelic and biallelic deletions of 13q14 in a group of CLL/SLL patients investigated by CGH Haematological Cancer and SNP array (8x60K)

Fig. 2

CytoSure Haematological Cancer and SNP array of two cases: 25 (a) and 29 (b). The overview window shows ideogram of chromosome 13, below result of aCGH as a copy number variations (CNV) indicating deletion of 13q14, underneath big red blocks demonstrating uniparental disomy (UPD) regions revealed in SNP analysis. Lower section shows magnification of aCGH analysis (CNV)

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Molecular Cytogenetics

ISSN: 1755-8166