Product Details

Assay Reference Genome
Location

Chr.11:47488887 on build GRCh38
Cytoband
11p11.2
Species
Homo sapiens
Variation Type
Copy Number

Additional Information

Target Gene Details

Entrez Gene ID
10658
Gene Symbol
CELF1
Gene Name
CUGBP, Elav-like family member 1
Gene Aliases
BRUNOL2, CUG-BP, CUGBP, CUGBP1, EDEN-BP, NAB50, NAPOR, hNab50
Location
Chr.11:47465937-47565569 on build GRCh38
Assay Gene Location
Within Exon 10
Gene Symbol Transcript Accession Exon Location Assay Location Protein ID
CELF1 NM_001025596.2 1 138 NP_001020767.1
NM_001172639.1 4 1103 NP_001166110.1
NM_001172640.1 1 138 NP_001166111.1
NM_006560.3 2 387 NP_006551.1
NM_198700.2 2 329 NP_941989.1
XM_011519848.2 2 210 XP_011518150.1
XM_011519850.2 2 449 XP_011518152.2
XM_011519852.2 4 558 XP_011518154.1
XM_011519854.1 6 666 XP_011518156.1
XM_011519855.1 2 387 XP_011518157.1
XM_011519856.1 3 468 XP_011518158.1
XM_011519857.1 2 339 XP_011518159.1
XM_011519858.1 2 434 XP_011518160.1
XM_011519859.1 6 666 XP_011518161.1
XM_017017101.1 5 550 XP_016872590.1
XM_017017102.1 4 469 XP_016872591.1
XM_017017103.1 3 362 XP_016872592.1
XM_017017104.1 3 362 XP_016872593.1
XM_017017105.1 3 362 XP_016872594.1
XM_017017106.1 5 550 XP_016872595.1
XM_017017107.1 3 362 XP_016872596.1
XM_017017108.1 3 362 XP_016872597.1
XM_017017109.1 2 449 XP_016872598.1
XM_017017110.1 3 362 XP_016872599.1
XM_017017111.1 3 362 XP_016872600.1
XM_017017112.1 3 362 XP_016872601.1
XM_017017113.1 3 362 XP_016872602.1
XM_017017114.1 3 362 XP_016872603.1
XM_017017115.1 4 390 XP_016872604.1
XM_017017116.1 3 425 XP_016872605.1
XM_017017117.1 2 186 XP_016872606.1
XM_017017118.1 2 308 XP_016872607.1
XM_017017119.1 4 527 XP_016872608.1
XM_017017120.1 2 339 XP_016872609.1
XM_017017121.1 2 434 XP_016872610.1
XM_017017122.1 2 339 XP_016872611.1
XM_017017123.1 2 387 XP_016872612.1
XM_017017124.1 4 481 XP_016872613.1
XM_017017125.1 2 210 XP_016872614.1
XM_017017126.1 2 339 XP_016872615.1
XM_017017127.1 2 363 XP_016872616.1
XM_017017128.1 2 387 XP_016872617.1
XM_017017129.1 3 385 XP_016872618.1
XM_017017130.1 2 339 XP_016872619.1
XM_017017131.1 2 363 XP_016872620.1
XM_017017132.1 2 387 XP_016872621.1
XM_017017133.1 2 178 XP_016872622.1
XM_017017134.1 3 317 XP_016872623.1
XM_017017135.1 2 339 XP_016872624.1
AB210019.1 4 1103
AF248648.1 1 146 AAF86230.1
AF267533.1 1 139 AAF78955.1
AF267534.1 1 139 AAF78956.1
AJ007988.1 1 128 CAC20566.1
AK304430.1 1 81
BC031079.1 2 329 AAH31079.1
CB960956.1 3 290
DA217269.1 4 410
DA320861.1 2 388
DB162286.1 2 287
U63289.1 2 265 AAC50895.1

Target Copy Number Variation Details

DGV Version
Release date: 2016-05-15, GRCh GRCh38
Target
Variation
Location CNV
Subtype
Genes
nsv832141 Chr11:47311629 - 47499441 on Build GRCh38 Loss SLC39A13 MIR4487 MADD RAPSN MYBPC3 PSMC3 SPI1 CELF1

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