Fig. 2
From: Copy number variations in Saudi family with intellectual disability and epilepsy
Array-CGH profiles analysis using Agilent CytoGenomic Analytics software (V.3.0.6.6) showing the deletion. Zero value indicates equal fluorescence intensity ratio between the sample and reference. Copy number losses shifted the ratio toward left (red), whereas copy number gains towards the right side (blue). CNV deletions observed in the chromosomal regions 8p23-p21 in four affected members of the family starts from 4,303,127 end 4,337,759 and the potential gene in this region is CSMD1 (OMIM: 612279)