A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996301



Internal ID15235161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:10678454..12678453hg38UCSC Ensembl
Outerchr11:10700001..12700000hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg382000000
hg192000000
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483000
Supporting Variants
Samples
Known GenesCSNK2A3, CTR9, DKK3, EIF4G2, GALNT18, MICAL2, MICALCL, MIR4299, MIR6124, MIR8070, MRVI1, PARVA, SNORD97, TEAD1, USP47, ZBED5, ZBED5-AS1
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996301
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer