Variant Details

Variant: esv3627950

Internal ID

6668094

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr11:122917874..122918922	hg38	UCSC Ensembl
Inner	chr11:122917875..122918922	hg38	UCSC Ensembl
Outer	chr11:122917874..122918923	hg38	UCSC Ensembl
	chr11:122788582..122789630	hg19	UCSC Ensembl
Inner	chr11:122788583..122789630	hg19	UCSC Ensembl
Outer	chr11:122788582..122789631	hg19	UCSC Ensembl

Cytoband

11q24.1

Allele length

Assembly	Allele length
hg38	1049
hg19	1049

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv14298952, essv14299025, essv14298971, essv14299015, essv14298941, essv14298960, essv14298986, essv14298946, essv14298987, essv14298959, essv14298980, essv14298992, essv14299027, essv14299008, essv14299045, essv14298958, essv14298947, essv14299037, essv14298993, essv14298944, essv14299038, essv14299023, essv14299007, essv14299004, essv14298964, essv14299036, essv14299013, essv14299002, essv14299021, essv14299019, essv14299026, essv14299014, essv14299033, essv14298957, essv14298949, essv14298998, essv14298953, essv14299039, essv14299012, essv14298981, essv14298954, essv14299042, essv14298995, essv14298977, essv14298969, essv14298988, essv14299017, essv14299003, essv14298989, essv14298999, essv14298965, essv14298976, essv14298943, essv14298996, essv14299043, essv14298961, essv14299034, essv14299005, essv14298979, essv14298968, essv14298970, essv14298975, essv14298963, essv14299020, essv14299024, essv14298983, essv14298984, essv14298948, essv14299041, essv14298972, essv14298966, essv14298950, essv14299000, essv14298973, essv14298962, essv14299001, essv14299016, essv14298974, essv14299011, essv14299032, essv14299044, essv14298978, essv14298991, essv14299029, essv14299040, essv14298994, essv14299031, essv14298945, essv14299009, essv14298956, essv14299018, essv14298967, essv14298982, essv14299028, essv14298942, essv14299030, essv14298997, essv14299006, essv14299010, essv14299035, essv14298990, essv14299022, essv14298985, essv14298951, essv14298955

Samples

HG02339, HG03484, NA18924, HG02583, NA19204, HG03175, NA18917, HG02323, HG03455, HG03100, NA18504, HG03295, HG03515, NA20346, HG03193, HG03139, HG03478, HG03199, HG03074, HG03082, NA19379, HG03385, HG03135, HG02810, HG02952, HG02485, HG03091, HG02595, NA19916, NA18916, HG02854, HG03105, HG02054, HG03479, HG02922, NA19130, HG03079, HG02505, HG02281, HG02315, NA18874, HG02885, NA19317, HG01973, HG02588, NA19036, HG02571, HG03073, NA19200, HG02442, HG02977, NA19247, NA19437, HG03160, NA19707, NA19175, NA19462, NA18933, HG02449, HG03457, NA19788, HG03575, HG02470, HG02757, NA18879, NA19449, HG03388, NA19338, NA19095, NA19625, HG02484, NA19436, HG03461, NA20276, NA19712, NA19747, NA19473, HG03117, NA19331, NA20351, NA19144, NA19334, HG03469, HG03419, HG02771, HG03565, NA20348, HG02971, HG02974, HG02095, HG03157, HG02646, HG03049, HG02938, HG02107, NA19093, HG03351, HG03410, HG03538, NA18488, HG03072, NA19214, HG03166, NA19431, HG02760

Known Genes

C11orf63

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3627950

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	105
Observed Complex	0
Frequency	n/a