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Gene Symbol: BCL2L11
Assay Reference Genome Location: Chr.2:111125974 on build GRCh38
Cytoband: 2q13

Assay ID

Hs04587701_cn

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Catalog #	4400291
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Genomic Map
Assay Details
More Information

Assay Details

Target Gene Details

Entrez Gene ID:	10018
Gene Name:	BCL2 like 11
Gene Aliases:	BAM, BIM, BOD
Location:	Chr.2:111120914-111168445 on Build GRCh38
Assay Gene Location:	Within Intron 4

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
BCL2L11	NM_001204106.1			NP_001191035.1
	NM_001204107.1			NP_001191036.1
	NM_001204108.1			NP_001191037.1
	NM_001204109.1			NP_001191038.1
	NM_001204110.1			NP_001191039.1
	NM_001204111.1			NP_001191040.1
	NM_001204112.1			NP_001191041.1
	NM_001204113.1			NP_001191042.1
	NM_006538.4			NP_006529.1
	NM_138621.4			NP_619527.1
	NM_138622.3			NP_619528.1
	NM_138623.3			NP_619529.1
	NM_138624.3			NP_619530.1
	NM_138625.3			NP_619531.1
	NM_138626.3			NP_619532.1
	NM_138627.3			NP_619533.1
	NM_207002.3			NP_996885.1
	NM_207003.2			NP_996886.1
	XM_005263550.3			XP_005263607.1
	XM_005263551.2			XP_005263608.1
	XM_005263552.3			XP_005263609.1
	XM_005263553.2			XP_005263610.1
	XM_005263554.2			XP_005263611.1
	XM_005263555.3			XP_005263612.1
	XM_005263556.3			XP_005263613.1
	XM_005263557.4			XP_005263614.1
	XM_005263559.2			XP_005263616.1
	XM_005263561.3			XP_005263618.1
	XM_011510461.2			XP_011508763.1
	XM_011510464.2			XP_011508766.1
	XM_017003101.1			XP_016858590.1
	XM_017003102.1			XP_016858591.1
	AB071195.1			BAB78589.1
	AB071196.1			BAB78590.1
	AB071197.1			BAB78591.1
	AB071198.1			BAB78592.1
	AB071199.1			BAB78593.1
	AB071200.1			BAB78594.1
	AF032457.1			AAC39593.1
	AF032458.1			AAC39594.1
	AK290377.1
	AK291269.1
	AW629314.1
	AY305714.1			AAQ82546.1
	AY305715.1			AAQ82547.1
	AY305716.1			AAT34900.1
	AY352518.1			AAQ62569.1
	AY423441.1			AAQ99148.1
	AY423442.1			AAQ99149.1
	AY423443.1			AAQ99150.1
	AY428962.1			AAR06908.1
	BC033694.1			AAH33694.1
	DQ849200.1			ABI13589.1
	DQ849201.1			ABI13590.1
	DQ849202.1			ABI13591.1

Target Copy Number Variation Details

DGV Version:

Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
esv2667742	Chr.2:111125617 - 111128520 on Build GRCh38	Deletion	BCL2L11
esv2720516	Chr.2:111125626 - 111128526 on Build GRCh38	Deletion	BCL2L11
nsv521956	Chr.2:110634682 - 112341235 on Build GRCh38	Loss	BCL2L11 SNORD132 FBLN7 MIR4435-2HG LOC400997 ACOXL MIR4435-2 PAFAH1B1P2 ANAPC1 TMEM87B ZC3H8 BUB1 ZC3H6 MIR4771-2 MERTK
nsv582699	Chr.2:110763166 - 112172487 on Build GRCh38	Loss	BCL2L11 PAFAH1B1P2 FBLN7 ANAPC1 MIR4435-2HG LOC400997 TMEM87B ACOXL MIR4771-2 MIR4435-2 MERTK
nsv963952	Chr.2:111125682 - 111135485 on Build GRCh38	Deletion	BCL2L11
nsv834331	Chr.2:111054562 - 111247101 on Build GRCh38	Loss	BCL2L11 MIR4435-2HG LOC400997 ACOXL
nsv829619	Chr.2:111125561 - 111127798 on Build GRCh38	Loss	BCL2L11
esv3591978	Chr.2:111125619 - 111128553 on Build GRCh38	Loss	BCL2L11
dgv4047n100	Chr.2:110308696 - 112358403 on Build GRCh38	Loss	BCL2L11 SNORD132 FBLN7 MIR4435-2HG LIMS4 LOC400997 RGPD6 ACOXL MIR4435-2 PAFAH1B1P2 LINC01106 LOC105373553 ANAPC1 TMEM87B ZC3H8 LOC100288570 BUB1 ZC3H6 MIR4771-2 LOC105375809 MERTK

More Information

Set Membership:

Intragenic

Intronic

Non-exonic

DGV Variation

Gene Ontology Categories:

Function(s) Process(es)

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