Hs05259447_cn

• Gene Symbol: LOC105369438
• Assay Reference Genome Location: Chr.11:94559024 on build GRCh38
• Cytoband: 11q21

Target Gene Details

• Entrez Gene ID: 105369438
• Gene Name: uncharacterized LOC105369438
• Gene Aliases: -
• Location: Chr.11:94545332-94740355 on Build GRCh38
• Assay Gene Location: Within Intron 7

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
LOC105369438	NR_135093.1
	NR_135094.1
	BI522712.1
	DA410022.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv2671948	Chr.11:94349534 - 94645424 on Build GRCh38	Deletion	GPR83 LOC105369438 MIR548L FUT4 PIWIL4 C11orf97 MRE11A ANKRD49

More Information

Additional Information:

For this assay, SNP(s) [rs76114211] 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, Intronic, Non-exonic, DGV Variation