Fig. 2. Microarray data of the rarely reported pathogenic copy number variations verified in this study: Agilent Human Genome oligonucleotide CGH showing deletions of 2.98 Mb on 2p21p16.3 (A), 1.46 Mb on 3p21.31 (B), 4.22 Mb on 10p11.22p11.21 (C), and 3.3 Mb on 14q24.2 (D).