Figure 1From: De novo 2.3 Mb microdeletion of 1q32.2 involving the Van der Woude Syndrome locusResults from analysis with Affymetrix SNP 6.0 array viewed with Chromosome Analysis Suite. (A) Copy number loss for probes on 1q32.2 for the patient with VWS. (B) Analysis of the father’s genome for the 1q32.2 region. (C) Analysis of the mother’s genome for the 1q32.2 region.Back to article page