Variant Details

Variant: esv3597193

Internal ID

6984507

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr3:101693323..101700611	hg38	UCSC Ensembl
Inner	chr3:101693323..101700611	hg38	UCSC Ensembl
Outer	chr3:101692823..101701111	hg38	UCSC Ensembl
	chr3:101412167..101419455	hg19	UCSC Ensembl
Inner	chr3:101412167..101419455	hg19	UCSC Ensembl
Outer	chr3:101411667..101419955	hg19	UCSC Ensembl

Cytoband

3q12.3

Allele length

Assembly	Allele length
hg38	7289
hg19	7289

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv11088383, essv11088363, essv11088364, essv11088368, essv11088359, essv11088343, essv11088379, essv11088355, essv11088373, essv11088371, essv11088351, essv11088367, essv11088382, essv11088342, essv11088378, essv11088350, essv11088376, essv11088347, essv11088345, essv11088380, essv11088356, essv11088377, essv11088352, essv11088369, essv11088358, essv11088375, essv11088340, essv11088357, essv11088370, essv11088365, essv11088344, essv11088353, essv11088348, essv11088374, essv11088339, essv11088361, essv11088349, essv11088362, essv11088372, essv11088381, essv11088341, essv11088366, essv11088354, essv11088360, essv11088346

Samples

HG01985, NA19703, HG02583, NA19914, HG03449, HG02012, HG03295, HG03577, HG03372, HG03069, HG02769, NA19107, HG03199, NA19379, HG02541, HG02549, HG04214, NA19137, HG02461, NA19451, HG02819, NA19152, NA19184, HG02449, NA19236, HG03457, HG02757, NA18879, HG02817, NA18499, HG03571, NA19338, HG02585, HG02635, HG02675, NA19308, HG02557, HG02759, NA20276, HG03433, HG02970, HG03063, HG01914, HG02947, HG02760

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3597193

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	45
Observed Complex	0
Frequency	n/a