Variant Details

Variant: esv2758906

Internal ID

9634365

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chrY:10001565..10266944	hg38	UCSC Ensembl
Inner	chrY:9839174..10104553	hg19	UCSC Ensembl
Inner	chrY:10449174..10714553	hg18	UCSC Ensembl
Inner	chrY:10432535..10697914	hg17	UCSC Ensembl

Cytoband

Yp11.2

Allele length

Assembly	Allele length
hg38	265380
hg19	265380
hg18	265380
hg17	265380

Variant Type

CNV gain

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

esv2758601

Samples

NA12248, NA12762, NA19120, NA12003, NA18516, NA19000, NA19154, NA19101, NA12144, NA18913, NA19144, NA06994, NA18971, NA19223, NA19211, NA18620

Known Genes

Method

BAC aCGH

Analysis

Array images were acquired using an Agilent laser scanner (Agilent Technologies, UK). Fluorescence intensities and log2 ratio values were extracted using Bluefuse software (Bluegnome Ltd).

Platform

Agilent

Comments

Reference

Redon_et_al_2006

Pubmed ID

17122850

Accession Number(s)

esv2758906

Frequency

Sample Size	270
Observed Gain	16
Observed Loss	0
Observed Complex	0
Frequency	n/a