Variant Details

Variant: essv21959

Internal ID

9620290

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr22:25268441..25523810	hg38	UCSC Ensembl
Outer	chr22:25245058..25528745	hg38	UCSC Ensembl
Inner	chr22:25664408..25919777	hg19	UCSC Ensembl
Outer	chr22:25641025..25924712	hg19	UCSC Ensembl
Inner	chr22:23994408..24249777	hg18	UCSC Ensembl
Outer	chr22:23971025..24254712	hg18	UCSC Ensembl
Inner	chr22:23988962..24244331	hg17	UCSC Ensembl
Outer	chr22:23965579..24249266	hg17	UCSC Ensembl

Cytoband

22q11.23

Allele length

Assembly	Allele length
hg38	283688
hg19	283688
hg18	283688
hg17	283688

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv2756760

Supporting Variants

Samples

NA07000

Known Genes

CRYBB2P1, IGLL3P, LRP5L, MIR6817

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)

essv21959

Frequency

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