Variant Details

Variant: esv2759197

Internal ID

9981342

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr3:162753261..163025006	hg38	UCSC Ensembl
Inner	chr3:162471049..162742794	hg19	UCSC Ensembl
Inner	chr3:163953743..164225488	hg18	UCSC Ensembl
Inner	chr3:163953751..164225496	hg17	UCSC Ensembl

Cytoband

3q26.1

Allele length

Assembly	Allele length
hg38	271746
hg19	271746
hg18	271746
hg17	271746

Variant Type

CNV gain+loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

esv2757902

Samples

NA19141, NA12717, NA11830, NA11995, NA11829, NA12004, NA12248, NA12146, NA10857, NA12155, NA19171, NA10846, NA10854, NA07048, NA12762, NA12044, NA19128, NA10855, NA11993, NA19194, NA12753, NA10831, NA18579, NA11839, NA18912, NA18853, NA12707, NA12144, NA19132, NA10856, NA10859, NA12873, NA12763, NA19173, NA10860, NA18854, NA19129

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)

esv2759197

Frequency

Sample Size	270
Observed Gain	36
Observed Loss	1
Observed Complex	0
Frequency	n/a