Figure 2 | Journal of Human Genetics

Figure 2

From: Copy-number variations on the X chromosome in Japanese patients with mental retardation detected by array-based comparative genomic hybridization analysis

Figure 2

Results of array-CGH analysis with the X-tiling array in probands of 10 families in which candidate pCNVs were detected. Each dot represents the log2 ratio of a BAC, and arrows and circles indicate MR-associated duplications (ratio >0.4) and homozygous deletions (ratio <−0.7), respectively. Arrowheads indicate benign CNVs. The gray vertical lines represent the centromeric region for which no clones were available.

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