Figure 2.

Microdeletions of uncertain significance with some published link to neuropsychiatric disease observed in NIMH cases with both schizophrenia and epilepsy. Deletions on specific Agilent custom arrays for validation are shown involving an exon of DLG2, an exon of SLC1A1, an exon of GRIP1, and multiple genes at the 20p13 locus as labeled. The regions of deletion are demarcated by red rectangles. Each dot represents an oligonucleotide, green for deleted and black for normal copy number.

Stewart et al. BMC Medical Genetics 2011 12:154   doi:10.1186/1471-2350-12-154
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