Figure 2

CNVs detected by whole genome sequencing and array-based CGH by Do et al. [36]. The results from whole genome sequencing were from Complete Genomics and are given in the left half of the chromosomes. The results from the array-based CGH are on the right half of the chromosomes. Regions are highlighted for copy number gain (red) and loss (blue). The major events partial trisomy of chromosome 1 and 2, complete trisomy of chromosome 7, gain in 17q and loss in 22q were confirmed. (Generated using http://db.systemsbiology.net/gestalt/cgi-pub/genomeMapBlocks.pl).