Introducing GenetiSure Cyto CGH and CGH + SNP Microarrays

Focus on what matters

The GenetiSure Cyto CGH and CGH + SNP Microarrays are a set of designs with updated content for the detection of copy number variations (CNV) and copy-neutral loss of heterozygosity (cnLOH) in constitutional DNA samples extracted from a variety of sources such as blood, saliva, amniotic fluid and CVS.

The new arrays include:

Constitutional designs that focus on disease-associated regions
Genome-wide backbone coverage
High resolution SNP for LOH detection

Learn more

Up-to-date Content

Content includes clinically relevant data from ClinGen, ClinVar, OMIM and Development Disorder Genotype-Phenotype Database (DDG2P)

Download brochure

Identify Genetic Aberrations with Confidence

These microarrays are developed for cytogenetic research and clinical laboratories who perform pre- and postnatal analysis and require:

A curated backbone with coverage on telomeres and PAR regions to improve coverage of clinically relevant regions and improve data interpretation.
High-quality probes enable copy number changes and mosaicism detection with high specificity and sensitivity.
Free space on each array for easy customization to integrate laboratory specific genes or regions of interest.

Additional Resources

Learn About Spike-Ins for Sample Tracking

Learn how spike-in probes help avoid errors during sample processing.

Learn more

GentiSure Video

Watch this video to hear about the GenetiSure Cyto Microarrays, the latest addition to the Agilent Genomics family of innovative products.

Watch now

Customize with Ease

Free space on each array for easy customization to integrate your specific gene/region of interest using SureDesign.

Launch SureDesign

For Research Use Only. Not for use in diagnostic procedures.

Personal Data

* This field is required

First Name*

Last Name*

Company/Organization*

Address*

Address 2

City*

State/Province

Postal Code*

Country*

Language

Phone*

Email Address*

Job Level

Primary Job Function

Application Interest

Please help us to better understand your profile and send you only the information you are interested in:

Diagnostics & Genomics

Product Interest:

Product and technologies that you would like to receive information about or purchase

Next Generation Sequencing

Sample QC & Electrophoresis

QC Throughput (Samples/Week). Select what applies

Or indicate your QC instrument:

Gene Expression & Cytogenomics

CRISPR gRNA Editing / Other Products

Other Products

I would like to be contacted by an Agilent representative

Any other questions, comments or suggestions?

Yes, I would like to receive email updates about Agilent products, services and events.

For full details of how we will treat your information please view our privacy policy: www.agilent.com/home/privacy-policy