Variant Details

Variant: essv25121

Internal ID

9623805

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr22:18903454..19018612	hg38	UCSC Ensembl
Outer	chr22:18903454..19043209	hg38	UCSC Ensembl
Inner	chr22:18890967..19006125	hg19	UCSC Ensembl
Outer	chr22:18890967..19030722	hg19	UCSC Ensembl
Inner	chr22:17270967..17386125	hg18	UCSC Ensembl
Outer	chr22:17270967..17410722	hg18	UCSC Ensembl
Inner	chr22:17265521..17380679	hg17	UCSC Ensembl
Outer	chr22:17265521..17405276	hg17	UCSC Ensembl

Cytoband

22q11.21

Allele length

Assembly	Allele length
hg38	139756
hg19	139756
hg18	139756
hg17	139756

Variant Type

CNV gain

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv2756758

Supporting Variants

Samples

NA10856

Known Genes

DGCR10, DGCR2, DGCR5, DGCR6, DGCR9, PRODH

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)

essv25121

Frequency

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