# New in Emedgene 2.16-2.19 (Dec 7, 2020)

Version 2.19 features improved CNV interpretation capabilities, most notably the ability to add a curated CNV database of chromosomal microarray results. We’ve also enhanced variant visualization, expanded *Preset* filter capabilities, and added the ability to reflex [*Case Type*](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/getting_around_the_platform/cases_tab/case_details) up to a broader testing option.

* **Add your curated CNV database**

You can now upload your own curated CNV database, even using historical microarray data. The data can be accessed through a corresponding filter under the [*Analysis tools*](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/reviewing_a_case/analysis-tools-tab/analysis_tools_tab) > [*Variant filters*](https://github.com/illumina-swi/emedgene-docs/blob/prod/docs/emedgene_analyze_manual/reviewing_a_case/variant_filters.md) in *Advanced mode* and in the [*Clinical Significance tab*](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/clinical_significance_section)*.*

* **Filter by CNV length**

We’ve added a *CNV Length* filter under the [*Quality filter*](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/reviewing_a_case/analysis-tools-tab/analysis_tools_tab/filters_presets_panel/filters/quality_filters) to help you filter out small CNVs that are typically noise.

* **Improved visualization**

We’ve added gene names to [visualization](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/visualization_section) tracks. You can also conveniently expand/collapse transcripts through a new control panel on the right. Stay tuned for more visualization tracks coming soon.

![](https://1131024994-files.gitbook.io/~/files/v0/b/gitbook-x-prod.appspot.com/o/spaces%2FGCW0DnLlE7QjoZPNmKIi%2Fuploads%2Fgit-blob-4c3f56a7830d128f89f9ea3f4d95c30e2f880d4c%2Fnew_in_emedgene_216-219_-dec_7-_2020_1_unnamed%2B4.png?alt=media)

* **Reflex case type**

You can [expand to a broader genetic testing option](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/reviewing_a_case/reflex_genetic_testing) if the results of more targeted testing are inconclusive. You may reflex from *Custom Panel* to *Exome* or *Genome*, or from *Exome* to *Genome*.

To do this, you should change the *Case type* in [*Edit case info*](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/reviewing_a_case/editing_an_existing_case) flow, thereby rerunning the broader analysis.

* *Preset* **filters by test type**

Everyone’s favorite feature, *Preset* filters, is getting an upgrade. You can now create different *Preset* filters for each of your test types. We hope this will streamline analysis and save you lots of time.

* **Enhanced reporting**

Are you using our slick new customizable reporting module? We now support all test types AND all variant types. Let us know if you’d like a demo.

* **Support Help Center**

Our live support knowledge base is finally here! If you’re looking for clarifications we’ve loaded answers to our most frequently asked questions, and we will continue to add articles on a weekly basis. You can also conveniently chat with the support team or send us a message.

![](https://1131024994-files.gitbook.io/~/files/v0/b/gitbook-x-prod.appspot.com/o/spaces%2FGCW0DnLlE7QjoZPNmKIi%2Fuploads%2Fgit-blob-3b4860730713c6ea9ef7c4cc738da7a048d551fe%2Fnew_in_emedgene_216-219_-dec_7-_2020_2_unnamed%2B3.png?alt=media)

Support and the new Help Center are accessible at all times via the question mark icon on the platform top bar.

![](https://1131024994-files.gitbook.io/~/files/v0/b/gitbook-x-prod.appspot.com/o/spaces%2FGCW0DnLlE7QjoZPNmKIi%2Fuploads%2Fgit-blob-3a9f63a5d205dc2839604b95d0d1c37e25aa2373%2Fnew_in_emedgene_216-219_-dec_7-_2020_3_unnamed%2B5.png?alt=media)