Research Article

Integrated Genomic Analysis of Sézary Syndrome

Figure 2

Illustration of an ideogram of genomewide SNP copy number changes in 8 SS cases identified by using Affymetrix GeneChip Human Mapping 10K Array as above and analysed with the IdeogramBrowser Software (http://www.informatik.uni-ulm.de/ni/staff/HKestler/ideo/doc.html). Here each red-coloured dot represents copy number loss of individual SNP and green-coloured dot stands for SNP copy number gain. Frequent SNP copy number changes at chromosomes 1, 2p, 3, 4q, 5q, 6, 7p, 8, 9, 10, 11, 12q, 13, 14, 16q, 17, and 20 are clearly visible.
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