The importance of copy numbers in genetic diagnostics and research
Copy number variants play a role in many genetic disorders. The fast, accurate and affordable detection of CNVs is essential for clinical genetic testing and research.
MRC Holland develops tools for the detection of DNA copy numbers and methylation patterns associated with disease. Our MLPA® technique is the gold standard in this field, and is used around the world to study hereditary disorders and tumours.
Latest News
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Feb 17, 2026New Product: NXtec D028 Carrier Panel 1
We are proud to introduce NXtec D028 Carrier Panel 1 - a high-throughput assay detecting CNVs and selected SNVs for carrier status analysis.
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Feb 16, 2026Our Products are IVDR-Certified!
We have successfully obtained our certification under the new In Vitro Diagnostic Regulation (IVDR; 2017/746)! The first batch of flagship products are already available on the market under the new IVDR, well in advance of the transition period deadline.
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Dec 19, 2025Changes to Our Product Packaging
Our product packaging will receive updates which simplify processing and pave the way for future innovations – there are no changes to the product contents.
Come and Meet Us
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Mar 04, 2026 - Munich, Germany
Visit us at GfH
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Mar 10, 2026 - Baltimore, USA
Visit us at ACMG
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Mar 17, 2026 - 12:00–16:00 CET
Virtual Workshop: MLPA Raw Data Evaluation and Troubleshooting
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Mar 31, 2026 - 12:00–16:00 CET
Virtual Workshop: MLPA Data Analysis and Quality Control with Coffalyser.Net