Hs01511268_cn

• Gene Symbol: LINC01124
• Assay Reference Genome Location: Chr.2:170713620 on build GRCh38
• Cytoband: 2q31.1

Target Gene Details

• Entrez Gene ID: 440925
• Gene Name: long intergenic non-protein coding RNA 1124
• Gene Aliases: -
• Location: Chr.2:170712439-170714567 on Build GRCh38
• Assay Gene Location: Within Exon 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
LINC01124	NR_027433.1	1	948
	AK123485.1	1	948	BAC85625.1

Target Gene Details

• Entrez Gene ID: 101926913
• Gene Name: uncharacterized LOC101926913
• Gene Aliases: -
• Location: Chr.2:170700368-170770766 on Build GRCh38
• Assay Gene Location: Within Intron 5

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
LOC101926913	NR_110185.1
	BM931568.1

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
esv26289	Chr.2:170713380 - 170717552 on Build GRCh38	Loss	LOC101926913 SP5 LINC01124
dgv7158n54	Chr.2:170712123 - 170717019 on Build GRCh38	Loss	LOC101926913 SP5 LINC01124
nsv821786	Chr.2:170711270 - 170718197 on Build GRCh38	Gain	LOC101926913 SP5 LINC01124

More Information

Additional Information:

For this assay, SNP(s) [rs72885464] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

• Set Membership: Intragenic, Exonic, Intronic, Non-exonic, DGV Variation