GENETIC ENCYCLOPEDIA
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GRCh37/hg19 11p15.4(chr11:7418934-8308834)x3 AND not provided

Significance: Uncertain significance
ClinVar: RCV000683352

Variant: GRCh37/hg19 11p15.4(chr11:7418934-8308834)x3

Type: Variant
Allele: GRCh37/hg19 11p15.4(chr11:7418934-8308834)x3 555047
Gene:
Type: copy number gain
Location: Chr11: 7418934 - 8308834 - assembly GRCh37

Condition

Disease: not provided