Variant Details

Variant: esv3587974

Internal ID

6975398

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr1:175053331..175057068	hg38	UCSC Ensembl
Inner	chr1:175053331..175057068	hg38	UCSC Ensembl
Outer	chr1:175053016..175057358	hg38	UCSC Ensembl
	chr1:175022467..175026204	hg19	UCSC Ensembl
Inner	chr1:175022467..175026204	hg19	UCSC Ensembl
Outer	chr1:175022152..175026494	hg19	UCSC Ensembl

Cytoband

1q25.1

Allele length

Assembly	Allele length
hg38	3738
hg19	3738

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv10189924, essv10189973, essv10189971, essv10189920, essv10189975, essv10189931, essv10189926, essv10189939, essv10189950, essv10189948, essv10189964, essv10189892, essv10189908, essv10189928, essv10189983, essv10189904, essv10189937, essv10189901, essv10189919, essv10189910, essv10189915, essv10189934, essv10189952, essv10189977, essv10189933, essv10189907, essv10189965, essv10189972, essv10189967, essv10189918, essv10189959, essv10189961, essv10189914, essv10189905, essv10189894, essv10189911, essv10189970, essv10189935, essv10189917, essv10189893, essv10189916, essv10189943, essv10189955, essv10189906, essv10189954, essv10189897, essv10189899, essv10189922, essv10189903, essv10189962, essv10189938, essv10189925, essv10189979, essv10189969, essv10189921, essv10189898, essv10189974, essv10189887, essv10189976, essv10189886, essv10189930, essv10189923, essv10189912, essv10189932, essv10189984, essv10189949, essv10189966, essv10189968, essv10189929, essv10189960, essv10189888, essv10189896, essv10189927, essv10189889, essv10189981, essv10189956, essv10189909, essv10189895, essv10189944, essv10189936, essv10189913, essv10189947, essv10189982, essv10189940, essv10189900, essv10189885, essv10189945, essv10189891, essv10189902, essv10189980, essv10189941, essv10189946, essv10189958, essv10189957, essv10189951, essv10189953, essv10189978, essv10189963, essv10189890, essv10189942

Samples

HG01985, HG01413, NA19028, HG02496, NA19909, HG03548, NA19399, NA19914, NA19332, HG03057, HG02337, NA18917, HG03115, NA19350, HG03130, HG02804, NA18878, HG03139, HG03172, NA19190, HG03372, HG03069, NA19446, HG03082, HG03452, NA18923, HG02840, HG02620, HG02854, HG02816, HG02981, HG03209, HG02561, HG03268, NA18868, NA19372, NA19385, HG03352, NA19722, NA19026, NA20412, NA19445, HG02882, HG03270, HG03048, HG03343, NA19908, HG01248, NA18934, HG03088, NA19462, NA19347, NA19152, HG03547, NA19184, HG02449, NA19391, NA19455, HG02953, HG03472, HG03301, NA19461, HG02817, NA18856, HG02884, HG02585, HG01890, HG01286, NA19318, HG03354, HG02594, HG03109, HG03064, HG02813, NA19017, HG03028, NA19440, HG02667, NA19108, NA19149, HG03117, NA19144, HG02314, HG03259, HG03127, NA19324, NA19310, HG02464, NA20281, NA19328, HG03039, HG03025, NA19468, HG03279, NA19900, HG02855, HG02465, HG02643, HG03271, HG03196

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3587974

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	100
Observed Complex	0
Frequency	n/a