Hs03793537_cn

• Gene Symbol: LOC338667
• Assay Reference Genome Location: Chr.11:125954968 on build GRCh38
• Cytoband: 11q24.2

Target Gene Details

• Entrez Gene ID: 338667
• Gene Name: V-set and immunoglobulin domain-containing protein 10-like
• Gene Aliases: -
• Location: Chr.11:125949191-125956319 on Build GRCh38
• Assay Gene Location: Within Intron 4

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
LOC338667	XM_017018652.1			XP_016874141.1
	XM_017018653.1			XP_016874142.1
	XM_017018654.1			XP_016874143.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv535	Chr.11:125918491 - 125963371 on Build GRCh38	Deletion	LOC338667 DDX25 CDON
nsv516919	Chr.11:125942455 - 125955813 on Build GRCh38	Loss	LOC338667
nsv556525	Chr.11:125690285 - 125971104 on Build GRCh38	Gain	PATE1 LOC338667 PATE3 LOC105369553 PUS3 PATE4 DDX25 PATE2 HYLS1 CDON
esv32964	Chr.11:125495069 - 126046387 on Build GRCh38	Gain+Loss	CHEK1 LOC338667 PATE3 PUS3 PATE4 DDX25 PATE2 HYLS1 CDON FEZ1 PATE1 LOC403312 LOC105369553 STT3A-AS1 STT3A EI24 ACRV1

More Information

Additional Information:

For this assay, SNP(s) [rs73019362,rs73019363] 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