GENETIC ENCYCLOPEDIA
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GRCh37/hg19 11p15.4(chr11:6969013-9257231)x3 AND not provided

Significance: Pathogenic
ClinVar: RCV000683360

Variant: GRCh37/hg19 11p15.4(chr11:6969013-9257231)x3

Type: Variant
Allele: GRCh37/hg19 11p15.4(chr11:6969013-9257231)x3 555055
Gene:
Type: copy number gain
Location: Chr11: 6969013 - 9257231 - assembly GRCh37

Condition

Disease: not provided