Copy Number & Structural Variant Analysis in Clinical Data | CNV, SV, Fusions, Validation

Clinical CNV/SV analysis end-to-end: panel/exome normalization, depth & log2 ratios, split-read/discordant pairs, fusions, QC thresholds, LoD studies, MLPA/FISH/ddPCR orthogonal confirmation, and audit-ready reporting.

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Copy Number & Structural Variant Analysis in Clinical Data — Hands-on

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