Figure 2 | Human Genome Variation

Figure 2

From: A de novo microdeletion in a patient with inner ear abnormalities suggests that the 10q26.13 region contains the responsible gene

Figure 2

The genome map around the 10q26.1 region. Deletion regions of the present patient and previously reported patients are depicted by bars. Deletions in patients with and without inner ear abnormalities are shown in red and blue, respectively. Dots at the end of the bars indicate more expansion of the deletions. A reticulated region indicates an ambiguous region due to the results obtained by conventional karyotyping. The genes discussed in the text are indicted by black rectangles. Proposed critical regions are designated by arrows.

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