Figure 5
From: Genetic and functional analysis of a Li Fraumeni syndrome family in China
The Copy Number Variations (CNVs) identified in the tumor samples from III:4 (A) and III:5 (B).
CNVs were analyzed with an Illumina Human Cyto SNP12, followed by Illumina’s Genome Studio Genotyping Module. The arrows indicated loss-of-heterozygosity (LOH) of chromosome 17, where TP53 gene was located.
