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Egyptian Journal of Medical Human Genetics
Fig. 2 | Egyptian Journal of Medical Human Genetics

Fig. 2

From: Identification of primary copy number variations reveal enrichment of Calcium, and MAPK pathways sensitizing secondary sites for autism

Fig. 2

a Karyogram of autism genes across populations. CNV burden is prominent in chromosomes 15, 16, and 18 across all the populations. Chromosome 15 has many CNV regions catering to the CNV burden. HapMap China, Tibetan and Ashkenazi Jews samples show specific CNV loci positioned at 2q21.1, 19p13, 20p11 and 13q14, respectively. The distribution of CNVs in sex chromosome varies in all the populations except for HapMap YRI and Tibetan populations where CNVs are absent. CNVs are absent in chromosomes 4, 14, 21, and Y. b Percentage of the top two prevalent autism genes: DUSP22 and ARHGAP11B across populations. HapMap JPT has the highest percentage of both the genes, while India has the least (0.8%)

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