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Fig. 1 | Journal of Neurodevelopmental Disorders

Fig. 1

From: CNTN6 copy number variations in 14 patients: a possible candidate gene for neurodevelopmental and neuropsychiatric disorders

Fig. 1

a aCGH profile showing an approximately 821-kb deletion in the 3p26.3 region (1,063,289–1,884,842) detected in patient 2; genome browser [hg18] showing the CNTN6 in the deleted region. b aCGH profile showing an approximately 541-kb duplication in the 3p26.3 region (855,662–1,397,384) detected in patient 9; genome browser [hg18] showing CNTN6 in the duplicated region

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