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Fig. 2 | Molecular Cytogenetics

Fig. 2

From: A chromosome 1q22 microdeletion including ASH1L is associated with intellectual disability in a Chinese family

Fig. 2

The SNP-array results of tested members from the Chinese family affected by intellectual disability. The proband (III-1), her father (II-2) and the fetus (IV-1) all contain a 936.3 kb heterozygous deletion of chromosome 1q22 (arr[GRCh37] 1q22 (155016052_155952375)×1). No significant CNVs were identified in the proband’s mother (II-1), grandparents (I-1 and -2) and paternal uncle II-3

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Molecular Cytogenetics

ISSN: 1755-8166