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Identification of Rare Recurrent Copy Number Variants in High-Risk Autism Families and Their Prevalence in a Large ASD Population

Figure 3

UCSC Genome browser view of CNVs in the NRXN1 region.

CNVs observed in the vicinity of the NRXN1-alpha transcription start site are shown. Note that most CNVs observed in ASD patients include exon 1 of NRXN1-alpha while only 1 control CNV extends into exon 1. Produced with custom tracks listing CNV calls and uploaded to http://genome.ucsc.edu.

Figure 3

doi: https://doi.org/10.1371/journal.pone.0052239.g003