Figure 4From: TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasiaSNP array genotyping confirming the 16p11.2 deletion. Five MA patients were confirmed with the 16p11.2 deletion using HumanOmni2.5-8 v1.0, Illumina. The patient samples are here shown together with a normal control sample (Genome Viewer, GenomeStudio V2011.1, Illumina).Back to article page