Variant Details

Variant: essv1541

Internal ID

9972577

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr12:61198700..61209729	hg38	UCSC Ensembl
Outer	chr12:61188514..61218770	hg38	UCSC Ensembl
Inner	chr12:61592481..61603510	hg19	UCSC Ensembl
Outer	chr12:61582295..61612551	hg19	UCSC Ensembl
Inner	chr12:59878748..59889777	hg18	UCSC Ensembl
Outer	chr12:59868562..59898818	hg18	UCSC Ensembl
Inner	chr12:59878748..59889777	hg17	UCSC Ensembl
Outer	chr12:59868562..59898818	hg17	UCSC Ensembl

Cytoband

12q14.1

Allele length

Assembly	Allele length
hg38	30257
hg19	30257
hg18	30257
hg17	30257

Variant Type

CNV gain

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv2757505

Supporting Variants

Samples

NA19012

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)

essv1541

Frequency

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