A curated catalogue of human genomic structural variation

Variant Details

Variant: nssv546019

Internal ID15206946
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:378188..641190hg38UCSC Ensembl
Innerchr11:378188..641190hg19UCSC Ensembl
Innerchr11:368188..631190hg18UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV loss
Copy Number1
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469923
Supporting Variants
Known GenesANO9, B4GALNT4, C11orf35, CDHR5, DRD4, HRAS, IRF7, LOC143666, LRRC56, MIR210, MIR210HG, PHRF1, PKP3, PTDSS2, RASSF7, RNH1, SCT, SIGIRR
MethodSNP array
AnalysisWe used the previously validated default quality control criteria, excluding samples with a log R ratio standard deviation of >0.28, a median B allele frequency of >0.55 or <0.45, or a B allele frequency drift of >0.002 (for more details see Wang et al. 2007). As the PennCNV algorithm is more sensitive and specific to CNVs covering greater numbers of SNPs in the HumanHap550 array, use of a minimum number of SNPs in CNV detection increases the reliability of CNV calls (with a consequent reduction in calls per individual). We set 10 SNPs as the minimum detection threshold in the algorithm.
PlatformIllumina HumanHap550 Genotyping BeadChip v3
Pubmed ID18288195
Accession Number(s)nssv546019
Sample Size443
Observed Gain0
Observed Loss1
Observed Complex0

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