A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049441



Internal ID18791972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55595852..55641874hg38UCSC Ensembl
Innerchr11:55363328..55409350hg19UCSC Ensembl
Innerchr11:55119904..55165926hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3846023
hg1946023
hg1846023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1175n100
Supporting Variantsnssv3709079, nssv3503646, nssv3513261, nssv3506563, nssv3520661, nssv3518277
Samples
Known GenesOR4C11, OR4P4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049441
Frequency
Sample Size29084
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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