GENETIC ENCYCLOPEDIA
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GRCh37/hg19 11p15.3(chr11:11461387-12258307)x1 AND not provided

Significance: Uncertain significance
ClinVar: RCV000845634

Variant: GRCh37/hg19 11p15.3(chr11:11461387-12258307)x1

Type: Variant
Allele: GRCh37/hg19 11p15.3(chr11:11461387-12258307)x1 672518
Gene:
Type: copy number loss
Location: Chr11: 11461387 - 12258307 - assembly GRCh37

Condition

Disease: not provided