Variant Details

Variant: essv22289

Internal ID

9620657

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr2:37733759..37762298	hg38	UCSC Ensembl
Outer	chr2:37733759..37762730	hg38	UCSC Ensembl
Inner	chr2:37960902..37989441	hg19	UCSC Ensembl
Outer	chr2:37960902..37989873	hg19	UCSC Ensembl
Inner	chr2:37814406..37842945	hg18	UCSC Ensembl
Outer	chr2:37814406..37843377	hg18	UCSC Ensembl
Inner	chr2:37872553..37901092	hg17	UCSC Ensembl
Outer	chr2:37872553..37901524	hg17	UCSC Ensembl

Cytoband

2p22.2

Allele length

Assembly	Allele length
hg38	28972
hg19	28972
hg18	28972
hg17	28972

Variant Type

CNV gain

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv2756917

Supporting Variants

Samples

NA12762

Known Genes

Method

SNP array

Analysis

The algorithm used to call CNVs using the 500K EA platform was developed to accurately define CNV regions using a large set of reference samples and is described in detail in a separate publication (Komura 2006). The algorithm contains three major parts: 1) Intensity pre-processing using an improved version of Genomic Imbalance Map (GIM) (Ishikawa et al. 2005), including probe selection, noise reduction, normalization, and intensity ratio adjustment based on affinity differences between alleles of a SNP, 2) CNV extraction, which identifies CNVs from all pair-wise comparisons using a modified SW-ARRAY, and 3) A copy number inference step which utilizes signal ratios and SNP information to more precisely define CNV boundaries and the copy number within each region.

Platform

Affymetrix GeneChip Early Access Mapping 500K Set Array (250K_Nsp_SNP)

Comments

Reference

Redon_et_al_2006

Pubmed ID

17122850

Accession Number(s)

essv22289

Frequency

Sample Size	270
Observed Gain	1
Observed Loss	0
Observed Complex	0
Frequency	n/a