Fig. 2From: 16p11.2 microdeletion syndrome: a case reportChromosome 16p11.2 deletion in our patient. The top panel shows the ideogram of chromosome 16 with the 16p11.2 (29592751-30,190,593) deleted region marked in a small red box. The scatter plot of the array-comparative genomic hybridization data, in the central panel, shows a 597.84 kb microdeletion of 16p11.2 in our patient. The University of California, Santa Cruz (GRCh37/hg19 assembly) genes in the overlapping region are shown in the bottom panelBack to article page