Variant Details

Variant: esv3588968

Internal ID

6976384

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr1:224136563..224139548	hg38	UCSC Ensembl
Inner	chr1:224136563..224139548	hg38	UCSC Ensembl
Outer	chr1:224136224..224139933	hg38	UCSC Ensembl
	chr1:224324265..224327250	hg19	UCSC Ensembl
Inner	chr1:224324265..224327250	hg19	UCSC Ensembl
Outer	chr1:224323926..224327635	hg19	UCSC Ensembl

Cytoband

1q42.11

Allele length

Assembly	Allele length
hg38	2986
hg19	2986

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv10306455, essv10306490, essv10306457, essv10306485, essv10306476, essv10306471, essv10306498, essv10306475, essv10306500, essv10306477, essv10306479, essv10306480, essv10306466, essv10306470, essv10306496, essv10306474, essv10306463, essv10306472, essv10306454, essv10306459, essv10306488, essv10306493, essv10306482, essv10306478, essv10306467, essv10306460, essv10306462, essv10306486, essv10306468, essv10306489, essv10306487, essv10306469, essv10306483, essv10306497, essv10306491, essv10306481, essv10306456, essv10306465, essv10306495, essv10306499, essv10306494, essv10306461, essv10306492, essv10306458, essv10306484, essv10306473, essv10306464

Samples

HG03514, HG03378, HG03300, HG03558, HG02476, HG03190, HG03295, NA20346, HG02621, HG03099, NA19307, HG02325, HG03246, HG02054, HG03224, HG02505, HG01067, NA19137, HG02885, NA19159, NA19026, HG02882, HG02479, HG02439, HG03054, HG03363, NA19462, HG01879, NA19982, HG02953, HG03563, NA19318, HG03354, NA19625, HG01896, NA19401, HG02807, HG03117, HG02580, HG03108, HG02771, HG02970, HG02938, HG03063, NA19102, NA19116, NA19463

Known Genes

FBXO28

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3588968

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	47
Observed Complex	0
Frequency	n/a