GENETIC ENCYCLOPEDIA
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GRCh37/hg19 11q23.3(chr11:116669751-120979377)x3 AND not provided

Significance: Likely pathogenic
ClinVar: RCV000683365

Variant: GRCh37/hg19 11q23.3(chr11:116669751-120979377)x3

Type: Variant
Allele: GRCh37/hg19 11q23.3(chr11:116669751-120979377)x3 555060
Gene:
Type: copy number gain
Location: Chr11: 116669751 - 120979377 - assembly GRCh37

Condition

Disease: not provided