A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2199n54



Internal ID20135623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130070036..130071126hg38UCSC Ensembl
chr11:129939931..129941021hg19UCSC Ensembl
chr11:129445141..129446231hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg381091
hg191091
hg181091
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556568, nsv556570
Samples
Known GenesAPLP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2199n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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