Figure 3
From: A complex microdeletion 17q12 phenotype in a patient with recurrent de novo membranous nephropathy
The heterozygous 1.43 Mb deletion arr 17q12(34.817.222-36.249.059)x1 (ISCN 2009, GRCh37/hg19) containing the sixteen RefSeq genes ZNHIT3, MYO19, PIGW, GGNBP2, DHRS11, MRM1, LHX1, AATF, ACACA, C17orf78, TADA2L, DUSP14, AP1GBP1, DDX52, HNF1β, LOC2841100, as detected by array-based comparative genomic hybridisation (Array-CGH, Oligo-Microarray Human Genome 244A; Agilent Technologies).