Variant Details

Variant: esv3586923

Internal ID

6974351

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr1:99425332..99426095	hg38	UCSC Ensembl
Inner	chr1:99425333..99426095	hg38	UCSC Ensembl
Outer	chr1:99425332..99426096	hg38	UCSC Ensembl
	chr1:99890888..99891651	hg19	UCSC Ensembl
Inner	chr1:99890889..99891651	hg19	UCSC Ensembl
Outer	chr1:99890888..99891652	hg19	UCSC Ensembl

Cytoband

1p21.2

Allele length

Assembly	Allele length
hg38	764
hg19	764

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv10028064, essv10028144, essv10028079, essv10028105, essv10028115, essv10028130, essv10028088, essv10028082, essv10028052, essv10028047, essv10028140, essv10028098, essv10028077, essv10028062, essv10028141, essv10028046, essv10028114, essv10028117, essv10028071, essv10028090, essv10028135, essv10028075, essv10028057, essv10028142, essv10028104, essv10028093, essv10028043, essv10028031, essv10028097, essv10028119, essv10028092, essv10028058, essv10028123, essv10028041, essv10028134, essv10028070, essv10028110, essv10028068, essv10028121, essv10028095, essv10028078, essv10028112, essv10028083, essv10028085, essv10028102, essv10028056, essv10028137, essv10028063, essv10028067, essv10028100, essv10028053, essv10028065, essv10028037, essv10028138, essv10028096, essv10028086, essv10028045, essv10028091, essv10028072, essv10028132, essv10028129, essv10028094, essv10028089, essv10028051, essv10028126, essv10028108, essv10028122, essv10028109, essv10028059, essv10028050, essv10028035, essv10028033, essv10028069, essv10028125, essv10028080, essv10028040, essv10028049, essv10028103, essv10028036, essv10028044, essv10028128, essv10028048, essv10028118, essv10028113, essv10028084, essv10028066, essv10028111, essv10028139, essv10028106, essv10028074, essv10028061, essv10028107, essv10028039, essv10028055, essv10028030, essv10028081, essv10028032, essv10028133, essv10028099, essv10028131, essv10028143, essv10028073, essv10028034, essv10028042, essv10028087, essv10028076, essv10028038, essv10028101, essv10028054, essv10028120, essv10028136, essv10028124, essv10028127, essv10028116, essv10028060

Samples

NA19394, HG02339, NA19028, NA19141, NA19397, HG02481, NA19909, HG03548, NA18861, HG03163, HG01885, NA19914, HG02702, HG03111, HG03449, NA18917, HG03130, HG03298, HG03518, HG03139, HG03172, HG02536, NA19443, HG03372, HG02895, NA19107, NA19446, NA19379, NA19201, NA19315, HG02952, HG02549, NA19197, NA18498, HG03040, HG02816, HG02143, HG01080, NA19383, HG03045, HG03195, NA19385, NA19209, NA19025, HG03583, HG03394, NA20318, HG03048, HG02439, NA19247, HG03160, HG02334, NA19175, NA19152, NA19184, HG02449, NA19327, HG01882, HG02144, HG03575, NA18871, HG02508, HG01880, HG01047, HG03301, NA19114, NA20299, NA19118, NA18856, NA19338, HG02979, HG03046, NA19225, HG01956, NA19035, HG02772, NA19017, HG02330, NA19440, HG02501, NA19019, HG02308, NA19435, NA19037, HG01958, NA19439, NA19428, HG03473, NA19360, HG03419, HG01342, NA19376, NA18501, HG03565, HG03112, NA19438, HG01912, HG03025, NA19713, NA19185, NA19102, HG02013, HG01883, NA18505, NA19129, NA19312, HG02851, NA19463, NA18522, HG03129, NA19346, NA19214, NA19153, HG03265, HG02760

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3586923

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	115
Observed Complex	0
Frequency	n/a