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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 2

Manhattan plot of CNVs called both by PennCNV and CNAM.

Association statistics across all regions covered on the Illumina custom array are shown. Since the array used was not a genome-wide array, the width of each chromosome on the plot is not proportional to the chromosome length. Adjacent chromosomes are displayed in alternating red and blue colors to aid in distinguishing them.

Figure 2

doi: https://doi.org/10.1371/journal.pone.0052239.g002