Figure 1From: Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients Displays log-R-ratio (LRR)/B-allele frequency (BAF) traces of the two significant regions, in addition to call start, call end, call length, probe count and probe median for; A) CN gain on chromosome 7q11.21 and B) CN Gain on chromosome 16p11.2. Back to article page