A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2129n54



Internal ID22770024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:99722154..99765452hg38UCSC Ensembl
chr11:99592885..99636183hg19UCSC Ensembl
chr11:99098095..99141393hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3843299
hg1943299
hg1843299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556110, nsv556109
Samples
Known GenesCNTN5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2129n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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