Variant Details

Variant: esv2671723

Internal ID

9591142

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr11:72139332..72177658	hg38	UCSC Ensembl
Outer	chr11:72139175..72177811	hg38	UCSC Ensembl
Inner	chr11:71850376..71888702	hg19	UCSC Ensembl
Outer	chr11:71850219..71888855	hg19	UCSC Ensembl

Cytoband

11q13.4

Allele length

Assembly	Allele length
hg38	38637
hg19	38637

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv6040915, essv5656141, essv6049173, essv5987277, essv5687254, essv5948370, essv5756129, essv5595750, essv5555364, essv6517605, essv6440977, essv5724795, essv5746530, essv6289371, essv6208071, essv6343804, essv6582359, essv5672617, essv6385440, essv5679874, essv5450470, essv6399713, essv5439096, essv5663386, essv5432907, essv5494244, essv6570754, essv5682703, essv5614914, essv5440763, essv6539931, essv6351428, essv6422142, essv5828964, essv6187848, essv6498793, essv5589047, essv5820695, essv6415156, essv5994548, essv6476966, essv6179782, essv5954277, essv6338623, essv6312009, essv5620600, essv5840439, essv6266644, essv6480012, essv6403195, essv5673192, essv5607529, essv5623105, essv6305490, essv6329166, essv6047034, essv5412348, essv6441937, essv6020501, essv5476516, essv6583859, essv6144074, essv5398095, essv6129120, essv5555140, essv5787501, essv6234311, essv5586032, essv6031605, essv5480465, essv6199899, essv6099257, essv6167321, essv6375638, essv6538045, essv6097087, essv5793487, essv5996444, essv5440996, essv5607751, essv6366805, essv6331189, essv5960085, essv6488822, essv5586681, essv6411731, essv5792380, essv6205149, essv5713234, essv6132440, essv5977093, essv5566513, essv6414280, essv6582454, essv5844243, essv5663568, essv6114295, essv6309592, essv5987214, essv5810881, essv6305584, essv6233438, essv6065649, essv6536370, essv5515288, essv6352077, essv6165489, essv5495329, essv6228026, essv6235405, essv5937956, essv6346962, essv5783039, essv6449160, essv6165178, essv5515100, essv6189912, essv5659838, essv5895159, essv5921827, essv5829792, essv5921193, essv5660259, essv6578530, essv5506670, essv6314175, essv6455694, essv5986001, essv6413989, essv6064469, essv5612787, essv5431147, essv6578504, essv5874687, essv5820888, essv5458322, essv6458158, essv6263176, essv5560352, essv5569236, essv6532781, essv5793256, essv6392514

Samples

NA18502, HG01060, HG00542, HG00442, NA20529, NA18947, HG00249, NA20508, HG00671, NA18592, NA10851, HG00187, NA18565, NA18507, NA18599, HG00233, HG00318, HG00566, NA19377, HG00449, NA20517, HG00261, NA07357, HG01140, NA18627, HG00327, NA07346, NA19068, NA19746, NA19373, HG01350, NA19379, NA18944, NA18940, NA18550, HG00251, HG00501, NA19762, HG00689, HG00448, HG00330, NA18547, HG01354, NA20540, NA19054, NA18498, NA19782, NA18964, NA11930, HG01069, HG00683, NA06984, NA12044, NA19731, NA18986, HG00182, HG00427, NA19901, HG00326, NA19789, NA18539, NA20818, NA11831, HG00543, HG00629, HG00443, NA18538, HG00282, NA20524, NA19403, NA12342, NA12003, NA19347, NA18956, HG00657, NA20536, NA19391, HG00436, NA19982, NA18948, NA19776, HG00708, NA19654, HG00324, HG01073, NA19114, NA11919, HG00690, HG00331, HG00684, NA18856, HG00140, HG01334, NA19338, NA18570, HG01107, NA18608, NA18953, NA19652, NA18542, NA19440, NA19390, NA18909, NA18952, NA18543, NA19147, NA18559, NA18517, HG00136, NA20520, NA07051, NA20785, NA12046, HG01357, NA20530, HG00237, NA19783, NA12763, HG01342, NA06986, HG00125, NA18501, HG00707, HG00672, HG00478, NA19779, NA12749, NA19093, HG00310, NA19780, NA18983, HG01251, NA20502, NA18505, HG01082, NA19758, NA20322, NA12890, NA20585, NA19065, NA20754, HG01061, HG00437

Known Genes

FOLR3

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2671723

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	143
Observed Complex	0
Frequency	n/a