A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3508895



Internal ID18460490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:34919190..37195907hg38UCSC Ensembl
Innerchr11:34940737..37217457hg19UCSC Ensembl
Innerchr11:34897313..37174033hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg382276718
hg192276721
hg182276721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042014
Supporting Variants
Samples
Known GenesC11orf74, CD44, COMMD9, FJX1, LDLRAD3, MIR1343, MIR3973, PAMR1, PDHX, PRR5L, RAG1, RAG2, SLC1A2, TRAF6, TRIM44
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3508895
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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