Fig. 2From: 19p13.2 Microdeletion including NFIX associated with overgrowth and intellectual disability suggestive of Malan syndromeHuman Omni1-Quad SNP-array result of the 19p13.2-p13.13 in Patient 1 with Malan syndrome. SNP-based array shows a de novo 1.4 Mb deletion (chr19: 12,157,839-13,518,462/hg19). Log R ratio and B allele frequencies are showed in upper panel; the lower panel shows genes in the deleted regionBack to article page