Variant Details

Variant: esv3626811

Internal ID

6666959

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr11:73203052..73203993	hg38	UCSC Ensembl
Inner	chr11:73203053..73203993	hg38	UCSC Ensembl
Outer	chr11:73203052..73203994	hg38	UCSC Ensembl
	chr11:72914097..72915038	hg19	UCSC Ensembl
Inner	chr11:72914098..72915038	hg19	UCSC Ensembl
Outer	chr11:72914097..72915039	hg19	UCSC Ensembl

Cytoband

11q13.4

Allele length

Assembly	Allele length
hg38	942
hg19	942

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv14212069, essv14212096, essv14212078, essv14212150, essv14212071, essv14212137, essv14212090, essv14212166, essv14212140, essv14212162, essv14212149, essv14212136, essv14212064, essv14212159, essv14212145, essv14212088, essv14212066, essv14212114, essv14212093, essv14212119, essv14212095, essv14212138, essv14212102, essv14212113, essv14212083, essv14212160, essv14212141, essv14212073, essv14212122, essv14212079, essv14212117, essv14212163, essv14212107, essv14212099, essv14212121, essv14212157, essv14212125, essv14212112, essv14212094, essv14212164, essv14212106, essv14212076, essv14212130, essv14212156, essv14212124, essv14212089, essv14212118, essv14212155, essv14212087, essv14212153, essv14212109, essv14212148, essv14212165, essv14212142, essv14212115, essv14212123, essv14212111, essv14212097, essv14212134, essv14212072, essv14212077, essv14212068, essv14212067, essv14212143, essv14212133, essv14212154, essv14212127, essv14212085, essv14212147, essv14212132, essv14212120, essv14212092, essv14212070, essv14212135, essv14212126, essv14212101, essv14212105, essv14212084, essv14212074, essv14212151, essv14212108, essv14212152, essv14212144, essv14212081, essv14212161, essv14212131, essv14212100, essv14212158, essv14212146, essv14212128, essv14212086, essv14212065, essv14212075, essv14212104, essv14212080, essv14212098, essv14212110, essv14212091, essv14212116, essv14212082, essv14212103, essv14212129, essv14212139

Samples

HG02890, HG03378, NA19204, HG03163, HG01885, HG02973, HG02891, HG02012, NA19092, HG02870, NA20298, HG03100, HG03295, NA20332, NA19377, HG03139, NA20356, HG03069, HG02769, HG03074, NA19379, HG03168, HG02952, HG02485, HG02541, HG02595, HG02549, HG03040, NA19923, NA18874, HG03268, HG02573, NA20340, HG02588, HG01440, HG02502, HG02427, HG03267, NA19209, HG02715, NA18867, NA20318, NA19027, HG03343, HG02439, HG03054, HG03061, HG03511, NA19175, NA19347, NA19984, NA19043, HG02554, HG03457, HG03575, HG02757, HG03472, HG01161, NA19042, HG03388, HG02309, NA20282, HG03451, HG03391, HG02979, HG02585, NA19756, NA19095, HG02586, HG03109, HG02568, HG02484, HG02722, HG02557, NA19108, NA19149, HG02759, NA20276, HG01915, NA19037, HG02923, NA19835, NA19310, NA19818, NA18501, HG02971, HG03442, HG02646, HG03279, HG02107, NA19185, HG02679, NA19116, NA19213, NA19900, HG01914, HG02763, HG01464, NA19312, HG03376, HG01886, HG02808, NA19153

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3626811

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	103
Observed Complex	0
Frequency	n/a