Fig. 2From: Prenatal diagnosis and genetic counseling of a 10p11.23q11.21 duplication associated with normal phenotypeCMA detected a 12.5-Mb chromosomal duplication in the region of 10p11.23q11.21 (arr[GRCh37]10p11.23q11.21(30,345,109_42,826,062) × 3)Back to article page