GENETIC ENCYCLOPEDIA
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GRCh37/hg19 11p15.1(chr11:17527585-18606820)x1 AND not provided

Significance: Uncertain significance
ClinVar: RCV000683355

Variant: GRCh37/hg19 11p15.1(chr11:17527585-18606820)x1

Type: Variant
Allele: GRCh37/hg19 11p15.1(chr11:17527585-18606820)x1 555050
Gene:
Type: copy number loss
Location: Chr11: 17527585 - 18606820 - assembly GRCh37

Condition

Disease: not provided