A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046402



Internal ID19135621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31600987..31662882hg38UCSC Ensembl
Innerchr11:31622534..31684430hg19UCSC Ensembl
Innerchr11:31579110..31641006hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3861896
hg1961897
hg1861897
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1090n100
Supporting Variantsnssv3510433, nssv3509331
Samples
Known GenesELP4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046402
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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