Product Details

Assay Reference Genome Location: Chr.X:41445681 on build GRCh38
Cytoband: Xp11.4
Species
Variation Type: Copy Number

Additional Information

For this assay, SNP(s) [rs139818142] 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.

Target Gene Details

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv508763	ChrX:41415959 - 41531609 on Build GRCh38	Insertion	CASK NYX
esv33720	ChrX:40891487 - 43157518 on Build GRCh38	Loss	LOC643043 DDX3X PPP1R2P9 GPR82 CASK LOC107985678 GPR34 USP9X LOC105373185 NYX

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