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GRCh37/hg19 11q14.1-14.3(chr11:81771852-90851187) AND Intellectual disability

Significance: Pathogenic
ClinVar: RCV000721939

Variant: GRCh37/hg19 11q14.1-14.3(chr11:81771852-90851187)

Type: Variant
Allele: GRCh37/hg19 11q14.1-14.3(chr11:81771852-90851187) 581732
Gene:
Type: copy number loss
Location: Chr11: 81771852 - 90851187 - assembly GRCh37

Condition

Finding: Intellectual disability