GENETIC ENCYCLOPEDIA
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GRCh37/hg19 11p12(chr11:40191196-40555598)x1 AND See cases

Significance: Uncertain significance
ClinVar: RCV000446576

Variant: GRCh37/hg19 11p12(chr11:40191196-40555598)x1

Type: Variant
Allele: GRCh37/hg19 11p12(chr11:40191196-40555598)x1 384195
Gene:
Type: copy number loss
Location: Chr11: 40191196 - 40555598 - assembly GRCh37
References: dbVar: nsv2778396
dbVar: nssv13653432

Condition

PhenotypeInstruction: See cases