Variant Details

Variant: esv3634962

Internal ID

7021762

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr14:75317916..75319276	hg38	UCSC Ensembl
Inner	chr14:75317936..75319257	hg38	UCSC Ensembl
Outer	chr14:75317897..75319296	hg38	UCSC Ensembl
	chr14:75784619..75785979	hg19	UCSC Ensembl
Inner	chr14:75784639..75785960	hg19	UCSC Ensembl
Outer	chr14:75784600..75785999	hg19	UCSC Ensembl

Cytoband

14q24.3

Allele length

Assembly	Allele length
hg38	1361
hg19	1361

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv15064102, essv15064096, essv15064020, essv15064107, essv15064033, essv15064025, essv15064074, essv15064064, essv15064016, essv15064062, essv15064032, essv15064067, essv15064045, essv15064092, essv15064029, essv15064083, essv15064115, essv15064007, essv15064002, essv15064019, essv15064118, essv15064111, essv15064097, essv15064030, essv15064108, essv15064031, essv15064040, essv15064104, essv15064091, essv15064109, essv15064028, essv15064058, essv15064036, essv15063998, essv15064066, essv15064106, essv15064052, essv15064027, essv15064103, essv15064024, essv15064090, essv15064100, essv15064003, essv15064077, essv15064023, essv15064122, essv15064123, essv15064078, essv15064050, essv15064088, essv15064000, essv15064069, essv15064051, essv15064087, essv15064037, essv15063999, essv15064081, essv15064017, essv15064120, essv15064015, essv15064121, essv15064099, essv15064053, essv15064006, essv15064071, essv15064070, essv15064124, essv15064014, essv15064061, essv15064044, essv15064095, essv15064116, essv15064042, essv15064114, essv15064012, essv15064009, essv15064101, essv15064073, essv15064105, essv15064013, essv15064093, essv15064080, essv15064063, essv15064022, essv15064035, essv15064034, essv15064110, essv15064055, essv15064043, essv15064065, essv15064057, essv15064026, essv15064089, essv15064084, essv15064048, essv15064039, essv15064010, essv15064072, essv15064021, essv15064098, essv15064086, essv15064079, essv15064082, essv15064046, essv15064059, essv15064008, essv15064094, essv15064068, essv15064060, essv15064005, essv15064018, essv15064038, essv15064011, essv15064047, essv15064076, essv15064112, essv15064113, essv15064041, essv15064119, essv15064001, essv15064117, essv15064075, essv15064049, essv15064085, essv15064056, essv15064054, essv15064004

Samples

HG02339, HG03366, HG03484, HG03121, HG03378, HG03163, HG02433, NA19704, HG03057, HG03241, NA19795, NA19350, HG03130, NA18486, HG03455, NA18878, NA20332, HG03577, NA19920, NA20359, HG03074, NA19374, HG03436, NA18519, NA19315, NA18489, HG03452, HG02952, HG02325, HG02756, NA19131, NA18916, HG03246, HG03040, NA19904, HG02111, NA19922, NA19404, HG03520, HG02703, HG02315, HG02573, NA18868, HG02634, HG01495, HG03212, HG02461, NA19235, NA19471, HG02588, NA20342, HG03583, NA18867, HG03369, NA19451, HG02716, HG01139, NA19247, NA19437, HG03160, HG03511, NA19175, NA19184, HG02511, NA19913, NA19455, HG02108, HG01077, NA18871, HG02968, HG02878, HG01889, HG03124, HG02555, NA18907, NA19114, NA19449, HG03382, HG02577, HG03078, HG01241, HG02309, HG03391, HG02979, NA19318, HG02332, NA19035, HG03567, HG03064, HG01363, HG01444, NA19390, HG03240, HG03437, NA20276, HG02010, HG02308, HG01894, NA19435, HG02837, HG02611, NA20362, NA18865, NA19835, NA19334, HG03259, HG03127, HG03419, HG03108, HG02558, NA19143, NA18501, HG02095, NA19716, HG02938, HG02053, HG02676, NA18873, HG03410, NA19116, HG02465, NA19463, HG02643, NA19153, HG03166, HG03271, HG03196

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3634962

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	127
Observed Complex	0
Frequency	n/a