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Chunk #10 — Results

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Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.
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We observed a significant excess of rare CNVs >100 kb in our ADHD case subjects relative to comparison subjects, with a rate 1.15 times higher and a proportion of subjects carrying at least one rare CNV >100 kb 1.13 times higher (Table 1). There was no significant evidence to suggest that the rare CNVs identified in the ADHD cases were on average longer than those identified in the comparison subjects, a finding in line with that of a previous study using a different data set (17). Limiting our analysis to the largest CNVs suggested that the higher rate in ADHD cases was strongest for rare CNVs >500 kb (1.28 times higher in the ADHD cases, p=0.032; Table 1). The rate of rare CNVs >500 kb observed in ADHD cases was 12.2%, which is in accordance with the rate of 12.5% reported in the previous study using analogous methodology and a different data set (17). While there was a difference in the gender distribution between the ADHD cases and the population-based comparison sample (which was 48% male), there was no significant